A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631828



Internal ID7018637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38954073..38955857hg38UCSC Ensembl
Innerchr13:38954085..38955846hg38UCSC Ensembl
Outerchr13:38954062..38955869hg38UCSC Ensembl
chr13:39528210..39529994hg19UCSC Ensembl
Innerchr13:39528222..39529983hg19UCSC Ensembl
Outerchr13:39528199..39530006hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381785
hg191785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14700775, essv14700776, essv14700774, essv14700760, essv14700748, essv14700749, essv14700762, essv14700777, essv14700754, essv14700770, essv14700759, essv14700756, essv14700771, essv14700763, essv14700750, essv14700765, essv14700766, essv14700778, essv14700753, essv14700755, essv14700769, essv14700751, essv14700752, essv14700761, essv14700767, essv14700773, essv14700764, essv14700757, essv14700772, essv14700758, essv14700768
SamplesHG01985, NA19909, HG03449, HG03130, HG02804, HG02476, NA19098, HG02769, HG03572, HG02620, NA20287, HG02981, NA19041, HG03520, HG02573, HG03394, HG02977, HG02449, NA19236, HG02307, HG01241, NA19099, HG02896, NA19324, HG02771, NA20357, NA19143, NA19474, NA19213, HG03129, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631828
Frequency
Sample Size2504
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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