A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016386



Internal ID19105605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136851152hg38UCSC Ensembl
Innerchr8:137687873..137863395hg19UCSC Ensembl
Innerchr8:137757055..137932577hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38175523
hg19175523
hg18175523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3690025, nssv3690026, nssv3690028, nssv3757492, nssv3690027, nssv3757491
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)nsv1016386
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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