A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027954



Internal ID19117172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:79224987..79321253hg38UCSC Ensembl
Innerchr8:80137222..80233488hg19UCSC Ensembl
Innerchr8:80299777..80396043hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3896267
hg1996267
hg1896267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7244n100
Supporting Variantsnssv3689584
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)nsv1027954
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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