A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691532



Internal ID18989813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131620467..131652625hg38UCSC Ensembl
Innerchr8:132632714..132664872hg19UCSC Ensembl
Innerchr8:132701896..132734054hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3832159
hg1932159
hg1832159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015649
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691532
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