A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149179



Internal ID15879959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63043867..63159995hg38UCSC Ensembl
Innerchr16:63077771..63193899hg19UCSC Ensembl
Innerchr16:61635272..61751400hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38116129
hg19116129
hg18116129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572885
Supporting Variants
SamplesNINDS_130
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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