A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527927



Internal ID18479522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66778307..66871735hg38UCSC Ensembl
Innerchr13:67352439..67445867hg19UCSC Ensembl
Innerchr13:66250440..66343868hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3893429
hg1993429
hg1893429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042756
Supporting Variants
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)nssv3527927
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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