A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696128



Internal ID15432780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9119327..9125205hg38UCSC Ensembl
Innerchr9:9119327..9125205hg19UCSC Ensembl
Innerchr9:9109327..9115205hg18UCSC Ensembl
Innerchr9:9109327..9115205hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg385879
hg195879
hg185879
hg175879
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518679
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696128
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