A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687478



Internal ID18985759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:50716059..50951075hg38UCSC Ensembl
Innerchr8:51628619..51863635hg19UCSC Ensembl
Innerchr8:51791172..52026188hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38235017
hg19235017
hg18235017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029698
Supporting Variants
Samples
Known GenesSNTG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3687478
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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