A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572916



Internal ID16013639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70123665..70236526hg38UCSC Ensembl
Innerchr16:70157568..70270429hg19UCSC Ensembl
Innerchr16:68715069..68827930hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38112862
hg19112862
hg18112862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859082
Samples
Known GenesCLEC18C, LOC100506060, PDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572916
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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