A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015463



Internal ID19104680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136849940hg38UCSC Ensembl
Innerchr8:137687873..137862183hg19UCSC Ensembl
Innerchr8:137757055..137931365hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38174311
hg19174311
hg18174311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3757486
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)nsv1015463
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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