A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026755



Internal ID19115973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102664742..102716328hg38UCSC Ensembl
Innerchr8:103676970..103728556hg19UCSC Ensembl
Innerchr8:103746146..103797732hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3851587
hg1951587
hg1851587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7278n100
Supporting Variantsnssv3691258
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)nsv1026755
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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