A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028809



Internal ID19118027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60076796..60095309hg38UCSC Ensembl
Innerchr8:60989355..61007868hg19UCSC Ensembl
Innerchr8:61151909..61170422hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3818514
hg1918514
hg1818514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7233n100
Supporting Variantsnssv3689461, nssv3689460
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)nsv1028809
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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