A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691468



Internal ID18989749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119338251..119353397hg38UCSC Ensembl
Innerchr8:120350491..120365637hg19UCSC Ensembl
Innerchr8:120419672..120434818hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3815147
hg1915147
hg1815147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015151
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)nssv3691468
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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