A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571049



Internal ID16358458
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 StatusM
Merged Variants
Supporting Variantsnssv1149283
SamplesHGDP00864
Known GenesLMF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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