A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020927



Internal ID18763461
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 StatusM
Merged Variants
Supporting Variantsnssv3685555, nssv3685554
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)nsv1020927
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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