A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030967



Internal ID19120187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137714848..137739157hg38UCSC Ensembl
Innerchr8:138727091..138751400hg19UCSC Ensembl
Innerchr8:138796273..138820582hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3824310
hg1924310
hg1824310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757497
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)nsv1030967
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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