A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520965



Internal ID15101572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37115199..37154796hg38UCSC Ensembl
Innerchr9:37115196..37154793hg19UCSC Ensembl
Innerchr9:37105196..37144793hg18UCSC Ensembl
Innerchr9:37105196..37144793hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3839598
hg1939598
hg1839598
hg1739598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678920, nssv681030
Samples
Known GenesZCCHC7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520965
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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