A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695952



Internal ID15432604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128825742..128826574hg38UCSC Ensembl
Innerchr10:130624006..130624838hg19UCSC Ensembl
Innerchr10:130513996..130514828hg18UCSC Ensembl
Innerchr10:130513996..130514828hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38833
hg19833
hg18833
hg17833
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518512
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695952
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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