A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518582



Internal ID15445875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4286736..4294414hg38UCSC Ensembl
Innerchr10:4328928..4336606hg19UCSC Ensembl
Innerchr10:4318928..4326606hg18UCSC Ensembl
Innerchr10:4318928..4326606hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg387679
hg197679
hg187679
hg177679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696027
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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