A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615433



Internal ID16402842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129396337..129415934hg38UCSC Ensembl
Innerchr9:132158616..132178213hg19UCSC Ensembl
Innerchr9:131198437..131218034hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3819598
hg1919598
hg1819598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176153
SamplesNINDS_71
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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