A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704408



Internal ID15094374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51628463..51640140hg38UCSC Ensembl
Innerchr10:53388223..53399900hg19UCSC Ensembl
Innerchr10:53058229..53069906hg18UCSC Ensembl
Innerchr10:53058229..53069906hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3811678
hg1911678
hg1811678
hg1711678
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527904
Supporting Variants
Samples
Known GenesPRKG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704408
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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