A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573130



Internal ID16013853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77921523..77996354hg38UCSC Ensembl
Innerchr16:77955420..78030251hg19UCSC Ensembl
Innerchr16:76512921..76587752hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3874832
hg1974832
hg1874832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv860790
Samples
Known GenesVAT1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573130
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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