A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674359



Internal ID15411011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635805..6803275hg38UCSC Ensembl
Innerchr10:6677767..6845237hg19UCSC Ensembl
Innerchr10:6717773..6885243hg18UCSC Ensembl
Innerchr10:6717773..6885243hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38167471
hg19167471
hg18167471
hg17167471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517486
Supporting Variants
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674359
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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