A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519386



Internal ID15446679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:154577719..154591203hg38UCSC Ensembl
Innerchr2:155434231..155447715hg19UCSC Ensembl
Innerchr2:155142477..155155961hg18UCSC Ensembl
Innerchr2:155259739..155273223hg17UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3813485
hg1913485
hg1813485
hg1713485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655771, nssv681740
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519386
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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