A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690095



Internal ID18641690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142430053..142601506hg38UCSC Ensembl
Innerchr8:143511414..143682867hg19UCSC Ensembl
Innerchr8:143508416..143679869hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38171454
hg19171454
hg18171454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033763
Supporting Variants
Samples
Known GenesBAI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690095
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer