A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522853



Internal ID15103460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59328164..59365421hg38UCSC Ensembl
Innerchr18:56995396..57032653hg19UCSC Ensembl
Innerchr18:55146376..55183633hg18UCSC Ensembl
Innerchr18:55146376..55183633hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3837258
hg1937258
hg1837258
hg1737258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698507
Samples
Known GenesLMAN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522853
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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