A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv853139



Internal ID16147095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23034551..23038125hg38UCSC Ensembl
Innerchr16:23045872..23049446hg19UCSC Ensembl
Innerchr16:22953373..22956947hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383575
hg193575
hg183575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571670
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv853139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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