A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699231



Internal ID15089197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9180514..9340901hg38UCSC Ensembl
Innerchr19:9291190..9451577hg19UCSC Ensembl
Innerchr19:9152190..9312577hg18UCSC Ensembl
Innerchr19:9152190..9312577hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38160388
hg19160388
hg18160388
hg17160388
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523472
Supporting Variants
Samples
Known GenesOR7D2, OR7D4, OR7E24, ZNF559, ZNF559-ZNF177, ZNF699
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699231
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer