A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522529



Internal ID15449822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:49150815..49194391hg38UCSC Ensembl
Innerchr18:46677185..46720761hg19UCSC Ensembl
Innerchr18:44931183..44974759hg18UCSC Ensembl
Innerchr18:44931183..44974759hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3843577
hg1943577
hg1843577
hg1743577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705901
Samples
Known GenesDYM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522529
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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