A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696601



Internal ID15086567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42710015..42715323hg38UCSC Ensembl
Innerchr6:42677753..42683061hg19UCSC Ensembl
Innerchr6:42785731..42791039hg18UCSC Ensembl
Innerchr6:42785731..42791039hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385309
hg195309
hg185309
hg175309
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519124
Supporting Variants
Samples
Known GenesPRPH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696601
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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