A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527930



Internal ID18826211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67279662..67482755hg38UCSC Ensembl
Innerchr13:67853794..68056887hg19UCSC Ensembl
Innerchr13:66751795..66954888hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38203094
hg19203094
hg18203094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046032
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527930
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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