A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029426



Internal ID19118645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136851152hg38UCSC Ensembl
Innerchr8:137681619..137863395hg19UCSC Ensembl
Innerchr8:137750801..137932577hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38181777
hg19181777
hg18181777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3689979, nssv3689978, nssv3689973, nssv3689981, nssv3689976, nssv3757476, nssv3757475, nssv3689974, nssv3689982, nssv3689986, nssv3689972, nssv3689975, nssv3689984, nssv3689977, nssv3757478, nssv3689985, nssv3689980, nssv3689983, nssv3757477
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)nsv1029426
Frequency
Sample Size11257
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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