A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689692



Internal ID18987973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88723405..89056620hg38UCSC Ensembl
Innerchr8:89735634..90068849hg19UCSC Ensembl
Innerchr8:89804750..90137965hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38333216
hg19333216
hg18333216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032038
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)nssv3689692
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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