A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691490



Internal ID18989771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:122449335..122467565hg38UCSC Ensembl
Innerchr8:123461574..123479804hg19UCSC Ensembl
Innerchr8:123530755..123548985hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3818231
hg1918231
hg1818231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021597
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)nssv3691490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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