A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13953891



Internal ID6276803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122051512..122062911hg38UCSC Ensembl
Innerchr10:122051548..122062875hg38UCSC Ensembl
Outerchr10:122051476..122062947hg38UCSC Ensembl
chr10:123811027..123822426hg19UCSC Ensembl
Innerchr10:123811063..123822390hg19UCSC Ensembl
Outerchr10:123810991..123822462hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624765
Supporting Variants
SamplesNA19792
Known GenesTACC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13953891
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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