A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526024



Internal ID15453317
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702254
Samples
Known GenesADCY9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526024
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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