A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685554



Internal ID18637149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:31140506..31162968hg38UCSC Ensembl
Innerchr8:30998022..31020484hg19UCSC Ensembl
Innerchr8:31117564..31140026hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3822463
hg1922463
hg1822463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020927
Supporting Variants
Samples
Known GenesWRN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685554
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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