A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701871



Internal ID15091837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139633261..139666176hg38UCSC Ensembl
Innerchr8:140645504..140678419hg19UCSC Ensembl
Innerchr8:140714686..140747601hg18UCSC Ensembl
Innerchr8:140714686..140747601hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3832916
hg1932916
hg1832916
hg1732916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525709
Supporting Variants
Samples
Known GenesKCNK9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701871
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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