A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696147



Internal ID15086113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86320473..86337398hg38UCSC Ensembl
Innerchr9:88935388..88952313hg19UCSC Ensembl
Innerchr9:88125208..88142133hg18UCSC Ensembl
Innerchr9:86164942..86181867hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3816926
hg1916926
hg1816926
hg1716926
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518696
Supporting Variants
Samples
Known GenesZCCHC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696147
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