A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573724



Internal ID16014447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89100686..89217401hg38UCSC Ensembl
Innerchr16:89167094..89283809hg19UCSC Ensembl
Innerchr16:87694595..87811310hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38116716
hg19116716
hg18116716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149665
SamplesHGDP00696
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)nsv573724
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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