A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696367



Internal ID15433019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130627275..130642501hg38UCSC Ensembl
Innerchr10:132425539..132440765hg19UCSC Ensembl
Innerchr10:132315529..132330755hg18UCSC Ensembl
Innerchr10:132315529..132330755hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3815227
hg1915227
hg1815227
hg1715227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516699
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696367
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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