A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572838



Internal ID16360247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60856408..60981773hg38UCSC Ensembl
Innerchr16:60890312..61015677hg19UCSC Ensembl
Innerchr16:59447813..59573178hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38125366
hg19125366
hg18125366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858910
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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