A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653188



Internal ID15043154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70660097..70741552hg38UCSC Ensembl
Innerchr16:70694000..70775455hg19UCSC Ensembl
Innerchr16:69251501..69332956hg18UCSC Ensembl
Innerchr16:69251501..69332956hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3881456
hg1981456
hg1881456
hg1781456
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesIL34, MTSS1L, VAC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653188
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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