A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573416



Internal ID16014139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83996684..84005144hg38UCSC Ensembl
Innerchr16:84030289..84038749hg19UCSC Ensembl
Innerchr16:82587790..82596250hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg388461
hg198461
hg188461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5260n54
Supporting Variantsnssv1149330
Samples1780854206_A
Known GenesNECAB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573416
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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