A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819929



Internal ID16113885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111029653..111096769hg38UCSC Ensembl
Innerchr13:111682000..111749116hg19UCSC Ensembl
Innerchr13:110480001..110547117hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3867117
hg1967117
hg1867117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563171
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819929
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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