A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149183



Internal ID15878964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64247705..64346933hg38UCSC Ensembl
Innerchr16:64281609..64380837hg19UCSC Ensembl
Innerchr16:62839110..62938338hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3899229
hg1999229
hg1899229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572898
Supporting Variants
SamplesHGDP01285
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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