A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001874



Internal ID19091091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108307017..108509733hg38UCSC Ensembl
Innerchr1:108849639..109052355hg19UCSC Ensembl
Innerchr1:108651162..108853878hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38202717
hg19202717
hg18202717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv250n100
Supporting Variantsnssv3483128
Samples
Known GenesNBPF6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001874
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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