A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527322



Internal ID15107929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51628463..51633338hg38UCSC Ensembl
Innerchr10:53388223..53393098hg19UCSC Ensembl
Innerchr10:53058229..53063104hg18UCSC Ensembl
Innerchr10:53058229..53063104hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384876
hg194876
hg184876
hg174876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703747
Samples
Known GenesPRKG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527322
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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