A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524215



Internal ID15451508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17950219..17993739hg38UCSC Ensembl
Innerchr8:17807728..17851248hg19UCSC Ensembl
Innerchr8:17852008..17895528hg18UCSC Ensembl
Innerchr8:17852008..17895528hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3843521
hg1943521
hg1843521
hg1743521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700102
Samples
Known GenesPCM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524215
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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