A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695465



Internal ID15085431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14475124..14476801hg38UCSC Ensembl
Innerchr8:14332633..14334310hg19UCSC Ensembl
Innerchr8:14377004..14378681hg18UCSC Ensembl
Innerchr8:14377004..14378681hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381678
hg191678
hg181678
hg171678
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known GenesSGCZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695465
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