A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149283



Internal ID15876584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:929006..945894hg38UCSC Ensembl
Innerchr16:979006..995894hg19UCSC Ensembl
Innerchr16:919007..935895hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816889
hg1916889
hg1816889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571049
Supporting Variants
SamplesHGDP00864
Known GenesLMF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149283
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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