A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031969



Internal ID19121191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142430053..142521484hg38UCSC Ensembl
Innerchr8:143511414..143602845hg19UCSC Ensembl
Innerchr8:143508416..143599847hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3891432
hg1991432
hg1891432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690094, nssv3690093
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)nsv1031969
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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