A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695353



Internal ID15432005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4058906..4065492hg38UCSC Ensembl
Innerchr16:4108907..4115493hg19UCSC Ensembl
Innerchr16:4048908..4055494hg18UCSC Ensembl
Innerchr16:4048908..4055494hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386587
hg196587
hg186587
hg176587
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517942
Supporting Variants
Samples
Known GenesADCY9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695353
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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