A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026385



Internal ID19115603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142392553..142521484hg38UCSC Ensembl
Innerchr8:143473914..143602845hg19UCSC Ensembl
Innerchr8:143471821..143599847hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38128932
hg19128932
hg18128027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7334n100
Supporting Variantsnssv3690090
Samples
Known GenesBAI1, TSNARE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026385
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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