A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573415



Internal ID16014138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83996684..84003076hg38UCSC Ensembl
Innerchr16:84030289..84036681hg19UCSC Ensembl
Innerchr16:82587790..82594182hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg386393
hg196393
hg186393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149329
SamplesHGDP00830
Known GenesNECAB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573415
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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