A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv853106



Internal ID15800376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21594646..21781111hg38UCSC Ensembl
Innerchr16:21605967..21792432hg19UCSC Ensembl
Innerchr16:21513468..21699933hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38186466
hg19186466
hg18186466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571634
Supporting Variants
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv853106
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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