A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527944



Internal ID18826225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68128624..68178080hg38UCSC Ensembl
Innerchr13:68702756..68752212hg19UCSC Ensembl
Innerchr13:67600757..67650213hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3849457
hg1949457
hg1849457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043587
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)nssv3527944
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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