A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028653



Internal ID19117871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136664978..136850192hg38UCSC Ensembl
Innerchr8:137677221..137862435hg19UCSC Ensembl
Innerchr8:137746403..137931617hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38185215
hg19185215
hg18185215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3692724, nssv3692725, nssv3692723
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)nsv1028653
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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