A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665197



Internal ID15401849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125378402..125410838hg38UCSC Ensembl
Innerchr10:127066971..127099407hg19UCSC Ensembl
Innerchr10:127056961..127089397hg18UCSC Ensembl
Innerchr10:127056961..127089397hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3832437
hg1932437
hg1832437
hg1732437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515901
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665197
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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