A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007990



Internal ID19097209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43124560..43148055hg38UCSC Ensembl
Innerchr4:43126577..43150072hg19UCSC Ensembl
Innerchr4:42821334..42844829hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3823496
hg1923496
hg1823496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625049
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007990
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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