A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149293



Internal ID15507721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58173299..58234532hg38UCSC Ensembl
Innerchr16:58207203..58268436hg19UCSC Ensembl
Innerchr16:56764704..56825937hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3861234
hg1961234
hg1861234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572763
Supporting Variants
Samples1780862101_A
Known GenesCSNK2A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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