A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13796115



Internal ID3797931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49074727..49075126hg38UCSC Ensembl
Innerchr10:49074757..49075096hg38UCSC Ensembl
Outerchr10:49074697..49075156hg38UCSC Ensembl
chr10:50282772..50283171hg19UCSC Ensembl
Innerchr10:50282802..50283141hg19UCSC Ensembl
Outerchr10:50282742..50283201hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623163
Supporting Variants
SamplesNA19681
Known GenesVSTM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13796115
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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