A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852522



Internal ID15799792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10018342..10090326hg38UCSC Ensembl
Innerchr16:10112199..10184183hg19UCSC Ensembl
Innerchr16:10019700..10091684hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3871985
hg1971985
hg1871985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571443
Supporting Variants
Samples
Known GenesGRIN2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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