A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524756



Internal ID15105363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139696474..139697714hg38UCSC Ensembl
Innerchr8:140708717..140709957hg19UCSC Ensembl
Innerchr8:140777899..140779139hg18UCSC Ensembl
Innerchr8:140777899..140779139hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381241
hg191241
hg181241
hg171241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700747
Samples
Known GenesKCNK9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524756
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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