A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689644



Internal ID18987925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84785707..84808064hg38UCSC Ensembl
Innerchr8:85697942..85720299hg19UCSC Ensembl
Innerchr8:85860497..85882854hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3822358
hg1922358
hg1822358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033771
Supporting Variants
Samples
Known GenesRALYL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689644
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