A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13752308



Internal ID2976159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35508831..35512021hg38UCSC Ensembl
Innerchr10:35508853..35511999hg38UCSC Ensembl
Outerchr10:35508809..35512043hg38UCSC Ensembl
chr10:35797759..35800949hg19UCSC Ensembl
Innerchr10:35797781..35800927hg19UCSC Ensembl
Outerchr10:35797737..35800971hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383191
hg193191
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622901
Supporting Variants
SamplesHG02628
Known GenesCCNY
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13752308
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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