A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689454



Internal ID18987735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:58188689..58228451hg38UCSC Ensembl
Innerchr8:59101248..59141010hg19UCSC Ensembl
Innerchr8:59263802..59303564hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3839763
hg1939763
hg1839763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024575
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)nssv3689454
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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