A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1144785



Internal ID15997971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129431819..129456077hg38UCSC Ensembl
Innerchr9:132194098..132218356hg19UCSC Ensembl
Innerchr9:131233919..131258177hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3824259
hg1924259
hg1824259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615434
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)nssv1144785
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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