A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13953794



Internal ID3955610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121712065..121717016hg38UCSC Ensembl
Innerchr10:121712106..121716975hg38UCSC Ensembl
Outerchr10:121712024..121717057hg38UCSC Ensembl
chr10:123471579..123476530hg19UCSC Ensembl
Innerchr10:123471620..123476489hg19UCSC Ensembl
Outerchr10:123471538..123476571hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384952
hg194952
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624758
Supporting Variants
SamplesHG03611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13953794
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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