A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516605



Internal ID15443898
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671088, nssv656395, nssv669506
Samples
Known GenesACSM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516605
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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