A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699037



Internal ID15089003
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523297
Supporting Variants
Samples
Known GenesPRKG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699037
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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