A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517926



Internal ID15445219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29284785..29302772hg38UCSC Ensembl
Innerchr10:29573714..29591701hg19UCSC Ensembl
Innerchr10:29613720..29631707hg18UCSC Ensembl
Innerchr10:29613720..29631707hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3817988
hg1917988
hg1817988
hg1717988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695337
Samples
Known GenesLYZL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517926
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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