A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852530



Internal ID15799800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11289662..11312946hg38UCSC Ensembl
Innerchr16:11383519..11406803hg19UCSC Ensembl
Innerchr16:11291020..11314304hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3823285
hg1923285
hg1823285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571454
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)nssv852530
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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