A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669506



Internal ID15406158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20660853..20661306hg38UCSC Ensembl
Innerchr16:20672175..20672628hg19UCSC Ensembl
Innerchr16:20579676..20580129hg18UCSC Ensembl
Innerchr16:20579676..20580129hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38454
hg19454
hg18454
hg17454
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516605
Supporting Variants
Samples
Known GenesACSM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669506
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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