A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705767



Internal ID15095733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98490429..98497603hg38UCSC Ensembl
Innerchr10:100250186..100257360hg19UCSC Ensembl
Innerchr10:100240176..100247350hg18UCSC Ensembl
Innerchr10:100240176..100247350hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg387175
hg197175
hg187175
hg177175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517710
Supporting Variants
Samples
Known GenesHPSE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705767
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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