A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019708



Internal ID19108926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110189986..110411829hg38UCSC Ensembl
Innerchr8:111202215..111424058hg19UCSC Ensembl
Innerchr8:111271391..111493234hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38221844
hg19221844
hg18221844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7282n100
Supporting Variantsnssv3691275
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)nsv1019708
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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