A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027485



Internal ID19116704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60076796..60095163hg38UCSC Ensembl
Innerchr8:60989355..61007722hg19UCSC Ensembl
Innerchr8:61151909..61170276hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3818368
hg1918368
hg1818368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7233n100
Supporting Variantsnssv3689456
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)nsv1027485
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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