A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051576



Internal ID18794107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66748615..66946123hg38UCSC Ensembl
Innerchr13:67322747..67520255hg19UCSC Ensembl
Innerchr13:66220748..66418256hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38197509
hg19197509
hg18197509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3527926
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051576
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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