A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv818821



Internal ID15766091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102820720..103931125hg38UCSC Ensembl
Innerchr13:103473070..104583475hg19UCSC Ensembl
Innerchr13:102271071..103381476hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg381110406
hg191110406
hg181110406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562981
Supporting Variants
Samples
Known GenesBIVM, BIVM-ERCC5, ERCC5, METTL21EP, MIR548AS, SLC10A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv818821
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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