A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673740



Internal ID15063706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13741945..13750800hg38UCSC Ensembl
Innerchr8:13599454..13608309hg19UCSC Ensembl
Innerchr8:13643825..13652680hg18UCSC Ensembl
Innerchr8:13643825..13652680hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388856
hg198856
hg188856
hg178856
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673740
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