A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697159



Internal ID15087125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4892019..4906729hg38UCSC Ensembl
Innerchr10:4934211..4948921hg19UCSC Ensembl
Innerchr10:4924211..4938921hg18UCSC Ensembl
Innerchr10:4924211..4938921hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814711
hg1914711
hg1814711
hg1714711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519977
Supporting Variants
Samples
Known GenesAKR1C6P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697159
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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