A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573726



Internal ID16014449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89114475..89197443hg38UCSC Ensembl
Innerchr16:89180883..89263851hg19UCSC Ensembl
Innerchr16:87708384..87791352hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3882969
hg1982969
hg1882969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5320n54
Supporting Variantsnssv863308
Samples
Known GenesACSF3, CDH15, LINC00304, LOC400558, SLC22A31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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