A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034672



Internal ID19123893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136848214hg38UCSC Ensembl
Innerchr8:137681619..137860457hg19UCSC Ensembl
Innerchr8:137750801..137929639hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38178839
hg19178839
hg18178839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3692750, nssv3692749
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)nsv1034672
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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