A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573674



Internal ID16014397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88738775..89325907hg38UCSC Ensembl
Innerchr16:88805183..89392315hg19UCSC Ensembl
Innerchr16:87332684..87919816hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38587133
hg19587133
hg18587133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863081
Samples
Known GenesACSF3, ANKRD11, APRT, CBFA2T3, CDH15, CDT1, GALNS, LINC00304, LOC100287036, LOC100289580, LOC400558, PABPN1L, PIEZO1, SLC22A31, TRAPPC2L, ZNF778
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573674
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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