A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572977



Internal ID16013700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74839615..74920999hg38UCSC Ensembl
Innerchr16:74873513..74954897hg19UCSC Ensembl
Innerchr16:73431014..73512398hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3881385
hg1981385
hg1881385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859179
Samples
Known GenesWDR59
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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