A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682481



Internal ID15419133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635805..6791647hg38UCSC Ensembl
Innerchr10:6677767..6833609hg19UCSC Ensembl
Innerchr10:6717773..6873615hg18UCSC Ensembl
Innerchr10:6717773..6873615hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38155843
hg19155843
hg18155843
hg17155843
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)nssv682481
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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