A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522839



Internal ID15450132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110612656..110618388hg38UCSC Ensembl
Innerchr1:111155278..111161010hg19UCSC Ensembl
Innerchr1:110956801..110962533hg18UCSC Ensembl
Innerchr1:110867320..110873052hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385733
hg195733
hg185733
hg175733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698491
Samples
Known GenesKCNA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522839
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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