A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852829



Internal ID15800099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16152307..16168715hg38UCSC Ensembl
Innerchr16:16246164..16262572hg19UCSC Ensembl
Innerchr16:16153665..16170073hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3816409
hg1916409
hg1816409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571550
Supporting Variants
Samples
Known GenesABCC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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