A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613736



Internal ID16401145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19914831..19943587hg38UCSC Ensembl
Innerchr9:19914829..19943585hg19UCSC Ensembl
Innerchr9:19904829..19933585hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3828757
hg1928757
hg1828757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156449
SamplesNINDS_125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613736
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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