A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv818847



Internal ID15766117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104426430..105664629hg38UCSC Ensembl
Innerchr13:105078780..106316978hg19UCSC Ensembl
Innerchr13:103876781..105114979hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg381238200
hg191238199
hg181238199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562996
Supporting Variants
Samples
Known GenesDAOA, DAOA-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv818847
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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