A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689999



Internal ID18988280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136837737hg38UCSC Ensembl
Innerchr8:137687873..137849980hg19UCSC Ensembl
Innerchr8:137757055..137919162hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38162108
hg19162108
hg18162108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033512
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)nssv3689999
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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