A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694579



Internal ID15431231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126471706..126525994hg38UCSC Ensembl
Innerchr10:128160275..128214563hg19UCSC Ensembl
Innerchr10:128150265..128204553hg18UCSC Ensembl
Innerchr10:128150265..128204553hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3854289
hg1954289
hg1854289
hg1754289
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521809
Supporting Variants
Samples
Known GenesC10orf90
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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