A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698186



Internal ID15434838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20553068..20609671hg38UCSC Ensembl
Innerchr16:20564390..20620993hg19UCSC Ensembl
Innerchr16:20471891..20528494hg18UCSC Ensembl
Innerchr16:20471891..20528494hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3856604
hg1956604
hg1856604
hg1756604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521570
Supporting Variants
Samples
Known GenesACSM2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698186
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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