A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034184



Internal ID19123406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:111159720..111262492hg38UCSC Ensembl
Innerchr8:112171949..112274721hg19UCSC Ensembl
Innerchr8:112241125..112343897hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38102773
hg19102773
hg18102773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757341
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)nsv1034184
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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