A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026039



Internal ID18768571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142430053..142616194hg38UCSC Ensembl
Innerchr8:143511414..143697555hg19UCSC Ensembl
Innerchr8:143508416..143694557hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38186142
hg19186142
hg18186142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7335n100
Supporting Variantsnssv3690096, nssv3690097, nssv3690098
Samples
Known GenesARC, BAI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026039
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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