A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572697



Internal ID16013420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57008367..57018072hg38UCSC Ensembl
Innerchr16:57042279..57051984hg19UCSC Ensembl
Innerchr16:55599780..55609485hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg389706
hg199706
hg189706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv857732
Samples
Known GenesNLRC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572697
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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