A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031946



Internal ID18774480
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 StatusM
Merged Variants
Supporting Variantsnssv3690051
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)nsv1031946
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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