A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042756



Internal ID18785287
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 StatusM
Merged Variants
Supporting Variantsnssv3527927
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)nsv1042756
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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