A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674294



Internal ID15410946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10614388..10617442hg38UCSC Ensembl
Innerchr10:10656351..10659405hg19UCSC Ensembl
Innerchr10:10696357..10699411hg18UCSC Ensembl
Innerchr10:10696357..10699411hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383055
hg193055
hg183055
hg173055
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517484
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674294
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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