A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519405



Internal ID15446698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26282850..26290933hg38UCSC Ensembl
Innerchr4:26284472..26292555hg19UCSC Ensembl
Innerchr4:25893570..25901653hg18UCSC Ensembl
Innerchr4:25960741..25968824hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388084
hg198084
hg188084
hg178084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684737, nssv683727, nssv655995
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519405
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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