A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572636



Internal ID16360045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55760694..55772968hg38UCSC Ensembl
Innerchr16:55794606..55806880hg19UCSC Ensembl
Innerchr16:54352107..54364381hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3812275
hg1912275
hg1812275
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv857491, nssv857492, nssv857490
Samples
Known GenesCES1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572636
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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