A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615560



Internal ID16402969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131393870..131395210hg38UCSC Ensembl
Innerchr9:134269257..134270597hg19UCSC Ensembl
Innerchr9:133259078..133260418hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381341
hg191341
hg181341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145313
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615560
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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