A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622909



Internal ID7009767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35928636..35931769hg38UCSC Ensembl
Innerchr10:35928636..35931769hg38UCSC Ensembl
Outerchr10:35928136..35932269hg38UCSC Ensembl
chr10:36217564..36220697hg19UCSC Ensembl
Innerchr10:36217564..36220697hg19UCSC Ensembl
Outerchr10:36217064..36221197hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383134
hg193134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13753910, essv13753908, essv13753909
SamplesHG00599, NA19000, HG01954
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622909
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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