A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520839



Internal ID15101446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36462132..36510652hg38UCSC Ensembl
Innerchr1:36927733..36976253hg19UCSC Ensembl
Innerchr1:36700320..36748840hg18UCSC Ensembl
Innerchr1:36596826..36645346hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3848521
hg1948521
hg1848521
hg1748521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697643
Samples
Known GenesCSF3R, MRPS15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520839
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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