A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702254



Internal ID15438906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4074299..4081882hg38UCSC Ensembl
Innerchr16:4124300..4131883hg19UCSC Ensembl
Innerchr16:4064301..4071884hg18UCSC Ensembl
Innerchr16:4064301..4071884hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387584
hg197584
hg187584
hg177584
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526024
Supporting Variants
Samples
Known GenesADCY9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702254
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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