A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633338



Internal ID7020147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100082044..100087984hg38UCSC Ensembl
Innerchr13:100082044..100087984hg38UCSC Ensembl
Outerchr13:100081544..100088484hg38UCSC Ensembl
chr13:100734298..100740238hg19UCSC Ensembl
Innerchr13:100734298..100740238hg19UCSC Ensembl
Outerchr13:100733798..100740738hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg385941
hg195941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14875703, essv14875706, essv14875717, essv14875728, essv14875704, essv14875720, essv14875702, essv14875726, essv14875714, essv14875715, essv14875705, essv14875727, essv14875713, essv14875721, essv14875718, essv14875723, essv14875711, essv14875716, essv14875725, essv14875722, essv14875709, essv14875707, essv14875729, essv14875710, essv14875701, essv14875719, essv14875724, essv14875708, essv14875712
SamplesHG02610, HG03175, HG03241, HG02836, NA20321, HG02624, HG03436, NA19319, NA20320, NA19916, NA19197, HG02922, HG01242, HG02143, HG03460, NA19917, NA19207, HG03058, NA19921, HG03270, HG02439, NA18910, HG03124, HG02813, NA19147, NA19712, HG03458, HG01577, HG03258
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633338
Frequency
Sample Size2504
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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