A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572973



Internal ID16360382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74364860..74367895hg38UCSC Ensembl
Innerchr16:74398758..74401793hg19UCSC Ensembl
Innerchr16:72956259..72959294hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg383036
hg193036
hg183036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859176, nssv859175
Samples
Known GenesLOC283922
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572973
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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