A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573408



Internal ID16014131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83902155..83902816hg38UCSC Ensembl
Innerchr16:83935760..83936421hg19UCSC Ensembl
Innerchr16:82493261..82493922hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38662
hg19662
hg18662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861993
Samples
Known GenesMLYCD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573408
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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