A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525541



Internal ID18823822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103077307..103123649hg38UCSC Ensembl
Innerchr13:103729657..103775999hg19UCSC Ensembl
Innerchr13:102527658..102574000hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3846343
hg1946343
hg1846343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045291
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)nssv3525541
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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