A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530497



Internal ID18482092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70898018..71772254hg38UCSC Ensembl
Innerchr13:71472150..72346386hg19UCSC Ensembl
Innerchr13:70370151..71244387hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38874237
hg19874237
hg18874237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038176
Supporting Variants
Samples
Known GenesDACH1, LINC00348
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530497
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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