A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572837



Internal ID16360246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60799161..60868919hg38UCSC Ensembl
Innerchr16:60833065..60902823hg19UCSC Ensembl
Innerchr16:59390566..59460324hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3869759
hg1969759
hg1869759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858909
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572837
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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