A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573127



Internal ID16360536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77651793..77677207hg38UCSC Ensembl
Innerchr16:77685690..77711104hg19UCSC Ensembl
Innerchr16:76243191..76268605hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3825415
hg1925415
hg1825415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv860789
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573127
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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