A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694496



Internal ID15431148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110455533..110465955hg38UCSC Ensembl
Innerchr10:112215291..112225713hg19UCSC Ensembl
Innerchr10:112205281..112215703hg18UCSC Ensembl
Innerchr10:112205281..112215703hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3810423
hg1910423
hg1810423
hg1710423
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520369
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694496
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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