A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515823



Internal ID15096430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6554280..6555115hg38UCSC Ensembl
Innerchr10:6596242..6597077hg19UCSC Ensembl
Innerchr10:6636248..6637083hg18UCSC Ensembl
Innerchr10:6636248..6637083hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38836
hg19836
hg18836
hg17836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664888, nssv683122
Samples
Known GenesPRKCQ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515823
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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