A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572698



Internal ID16013421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57092192..57092906hg38UCSC Ensembl
Innerchr16:57126104..57126818hg19UCSC Ensembl
Innerchr16:55683605..55684319hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38715
hg19715
hg18715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5139n54
Supporting Variantsnssv857733
Samples
Known GenesCPNE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572698
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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