A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691276



Internal ID18989557
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 StatusS
Merged Variantsnsv1032460
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)nssv3691276
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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