A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526199



Internal ID15453492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29287485..29290553hg38UCSC Ensembl
Innerchr10:29576414..29579482hg19UCSC Ensembl
Innerchr10:29616420..29619488hg18UCSC Ensembl
Innerchr10:29616420..29619488hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg383069
hg193069
hg183069
hg173069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702462
Samples
Known GenesLYZL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526199
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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