A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034768



Internal ID18777301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124310770..124469492hg38UCSC Ensembl
Innerchr8:125323011..125481733hg19UCSC Ensembl
Innerchr8:125392192..125550914hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38158723
hg19158723
hg18158723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691503
Samples
Known GenesRNF139-AS1, TMEM65, TRMT12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034768
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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