A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609974



Internal ID16397383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:5888330..6390723hg38UCSC Ensembl
Innerchr8:5745852..6248244hg19UCSC Ensembl
Innerchr8:5733260..6235652hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38502394
hg19502393
hg18502393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156816
SamplesNINDS_219
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609974
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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