A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684474



Internal ID15074440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21593859..21728953hg38UCSC Ensembl
Innerchr16:21605180..21740274hg19UCSC Ensembl
Innerchr16:21512681..21647775hg18UCSC Ensembl
Innerchr16:21512681..21647775hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38135095
hg19135095
hg18135095
hg17135095
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517713
Supporting Variants
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684474
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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