A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606882



Internal ID6993817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136541079..136545106hg38UCSC Ensembl
Innerchr5:136541079..136545106hg38UCSC Ensembl
Outerchr5:136540788..136545497hg38UCSC Ensembl
chr5:135876768..135880795hg19UCSC Ensembl
Innerchr5:135876768..135880795hg19UCSC Ensembl
Outerchr5:135876477..135881186hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384028
hg194028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12068728, essv12068743, essv12068732, essv12068734, essv12068711, essv12068723, essv12068702, essv12068696, essv12068736, essv12068755, essv12068759, essv12068764, essv12068758, essv12068692, essv12068719, essv12068705, essv12068747, essv12068729, essv12068753, essv12068698, essv12068761, essv12068707, essv12068746, essv12068708, essv12068763, essv12068710, essv12068700, essv12068716, essv12068742, essv12068718, essv12068701, essv12068697, essv12068709, essv12068693, essv12068756, essv12068751, essv12068731, essv12068714, essv12068717, essv12068752, essv12068760, essv12068748, essv12068754, essv12068712, essv12068725, essv12068720, essv12068706, essv12068745, essv12068727, essv12068730, essv12068713, essv12068722, essv12068715, essv12068733, essv12068726, essv12068695, essv12068724, essv12068757, essv12068694, essv12068737, essv12068741, essv12068740, essv12068721, essv12068699, essv12068750, essv12068749, essv12068704, essv12068703, essv12068744, essv12068735, essv12068762, essv12068739, essv12068691, essv12068690, essv12068765, essv12068738
SamplesHG02574, NA19701, HG03121, HG03378, NA19466, HG03247, NA18881, HG02012, NA18486, HG02870, HG03298, HG02536, NA19443, NA20356, NA20359, HG03199, HG03436, HG01503, HG03099, HG03135, HG02485, HG02840, NA19197, HG03578, HG03479, NA19681, HG02816, HG02981, HG02505, NA19922, HG02561, HG03268, NA19137, NA19172, HG02420, HG02502, NA18520, NA18908, NA19200, HG02819, HG03120, HG02439, NA19247, NA19175, HG02322, HG02953, NA20126, HG01880, HG01390, HG03136, HG03388, NA19031, HG02283, NA19318, HG02635, NA18858, HG02675, HG02484, HG01896, HG02813, HG02255, HG01444, NA19390, NA19108, NA19019, HG02308, HG03458, HG02941, HG01933, NA19360, HG03419, HG02938, HG02107, HG02763, HG02855, NA19214
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606882
Frequency
Sample Size2504
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer