A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713291



Internal ID19011572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103261304..103360796hg38UCSC Ensembl
Innerchr13:103913654..104013146hg19UCSC Ensembl
Innerchr13:102711655..102811147hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3899493
hg1999493
hg1899493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044331
Supporting Variants
Samples
Known GenesMIR548AS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713291
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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