A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022076



Internal ID19111294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136851683hg38UCSC Ensembl
Innerchr8:137687873..137863926hg19UCSC Ensembl
Innerchr8:137757055..137933108hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38176054
hg19176054
hg18176054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3690030, nssv3690029
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)nsv1022076
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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