A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571048



Internal ID16358457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:884180..933163hg38UCSC Ensembl
Innerchr16:934180..983163hg19UCSC Ensembl
Innerchr16:874181..923164hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3848984
hg1948984
hg1848984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149282
Samples1780862388_A
Known GenesLMF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571048
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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