A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149624



Internal ID15506697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21563897..21728953hg38UCSC Ensembl
Innerchr16:21575218..21740274hg19UCSC Ensembl
Innerchr16:21482719..21647775hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38165057
hg19165057
hg18165057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571628
Supporting Variants
Samples1780854129_A
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149624
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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