A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633299



Internal ID7020108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97757651..97758154hg38UCSC Ensembl
Innerchr13:97757651..97758154hg38UCSC Ensembl
Outerchr13:97757375..97758459hg38UCSC Ensembl
chr13:98409905..98410408hg19UCSC Ensembl
Innerchr13:98409905..98410408hg19UCSC Ensembl
Outerchr13:98409629..98410713hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869700, essv14869719, essv14869704, essv14869693, essv14869713, essv14869737, essv14869705, essv14869730, essv14869736, essv14869728, essv14869696, essv14869732, essv14869726, essv14869706, essv14869695, essv14869731, essv14869702, essv14869718, essv14869742, essv14869739, essv14869715, essv14869709, essv14869710, essv14869697, essv14869720, essv14869694, essv14869733, essv14869721, essv14869723, essv14869701, essv14869741, essv14869716, essv14869729, essv14869724, essv14869722, essv14869707, essv14869725, essv14869703, essv14869712, essv14869727, essv14869734, essv14869735, essv14869711, essv14869717, essv14869738, essv14869708, essv14869698, essv14869714, essv14869699, essv14869740
SamplesHG01986, HG03366, HG02583, NA19909, NA19399, NA19020, HG03130, HG02323, HG01465, NA19377, NA20356, HG03385, NA19307, HG02541, HG02645, HG03105, NA19404, NA19041, NA19383, NA20340, NA19921, HG02716, HG02009, NA19247, HG03061, NA19403, NA18933, NA19984, HG02968, NA18499, HG01107, NA19401, HG01444, NA19309, HG02282, HG01190, NA19019, NA19454, HG02314, HG02580, HG02317, NA19360, NA19472, HG02679, HG03077, NA19030, NA18488, NA19346, NA19431, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633299
Frequency
Sample Size2504
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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