A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615439



Internal ID16402848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129434252..129484733hg38UCSC Ensembl
Innerchr9:132196531..132247012hg19UCSC Ensembl
Innerchr9:131236352..131286833hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3850482
hg1950482
hg1850482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176154
SamplesNINDS_200
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615439
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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