A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615801



Internal ID16403210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134079705..134128468hg38UCSC Ensembl
Innerchr9:136944827..136993590hg19UCSC Ensembl
Innerchr9:135934648..135983411hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3848764
hg1948764
hg1848764
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176374
SamplesHGDP01249
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615801
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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