A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658424



Internal ID15395076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16464502..16476408hg38UCSC Ensembl
Innerchr10:16506501..16518407hg19UCSC Ensembl
Innerchr10:16546507..16558413hg18UCSC Ensembl
Innerchr10:16546507..16558413hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3811907
hg1911907
hg1811907
hg1711907
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515521
Supporting Variants
Samples
Known GenesPTER
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658424
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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