A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523297



Internal ID15103904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51502228..51502381hg38UCSC Ensembl
Innerchr10:53261988..53262141hg19UCSC Ensembl
Innerchr10:52931994..52932147hg18UCSC Ensembl
Innerchr10:52931994..52932147hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38154
hg19154
hg18154
hg17154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699037
Samples
Known GenesPRKG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523297
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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