A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13952845



Internal ID3945175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121118887..121122028hg38UCSC Ensembl
Innerchr10:121118922..121121993hg38UCSC Ensembl
Outerchr10:121118852..121122063hg38UCSC Ensembl
chr10:122878401..122881542hg19UCSC Ensembl
Innerchr10:122878436..122881507hg19UCSC Ensembl
Outerchr10:122878366..122881577hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624748
Supporting Variants
SamplesHG03598
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13952845
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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