A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699109



Internal ID15089075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66748582..66946212hg38UCSC Ensembl
Innerchr13:67322714..67520344hg19UCSC Ensembl
Innerchr13:66220715..66418345hg18UCSC Ensembl
Innerchr13:66220715..66418345hg17UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38197631
hg19197631
hg18197631
hg17197631
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523360
Supporting Variants
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699109
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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