A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016172



Internal ID19105390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:120667350..120917676hg38UCSC Ensembl
Innerchr8:121679590..121929916hg19UCSC Ensembl
Innerchr8:121748771..121999097hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38250327
hg19250327
hg18250327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691472
Samples
Known GenesSNTB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016172
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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