A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571429



Internal ID16358838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8916356..8983755hg38UCSC Ensembl
Innerchr16:9010213..9077612hg19UCSC Ensembl
Innerchr16:8917714..8985113hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3867400
hg1967400
hg1867400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150523
Samples1780862415_A
Known GenesUSP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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