A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032460



Internal ID19121682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110206628..110457882hg38UCSC Ensembl
Innerchr8:111218857..111470111hg19UCSC Ensembl
Innerchr8:111288033..111539287hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38251255
hg19251255
hg18251255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7282n100
Supporting Variantsnssv3691276
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)nsv1032460
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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