A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689867



Internal ID15426519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635805..6794725hg38UCSC Ensembl
Innerchr10:6677767..6836687hg19UCSC Ensembl
Innerchr10:6717773..6876693hg18UCSC Ensembl
Innerchr10:6717773..6876693hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38158921
hg19158921
hg18158921
hg17158921
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)nssv689867
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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