A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690051



Internal ID18641646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137096400..137289570hg38UCSC Ensembl
Innerchr8:138108643..138301813hg19UCSC Ensembl
Innerchr8:138177825..138370995hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38193171
hg19193171
hg18193171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031946
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)nssv3690051
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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