A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522354



Internal ID15102961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37985093..38021881hg38UCSC Ensembl
Innerchr3:38026584..38063372hg19UCSC Ensembl
Innerchr3:38001588..38038376hg18UCSC Ensembl
Innerchr3:38001588..38038376hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3836789
hg1936789
hg1836789
hg1736789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695133
Samples
Known GenesPLCD1, VILL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522354
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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