A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031976



Internal ID19121198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:111544242..111579153hg38UCSC Ensembl
Innerchr8:112556471..112591382hg19UCSC Ensembl
Innerchr8:112625647..112660558hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3834912
hg1934912
hg1834912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691299, nssv3691300
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)nsv1031976
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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