A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526411



Internal ID18824692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18683428hg38UCSC Ensembl
Innerchr13:19045628..19257568hg19UCSC Ensembl
Innerchr13:17943628..18155568hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38211941
hg19211941
hg18211941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051097
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)nssv3526411
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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