A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526602



Internal ID18824883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62927015..63181517hg38UCSC Ensembl
Innerchr13:63501148..63755650hg19UCSC Ensembl
Innerchr13:62399149..62653651hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38254503
hg19254503
hg18254503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054643
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)nssv3526602
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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