A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521690



Internal ID15102297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100465006..100734308hg38UCSC Ensembl
Innerchr14:100931343..101200645hg19UCSC Ensembl
Innerchr14:100001096..100270398hg18UCSC Ensembl
Innerchr14:100001096..100270398hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38269303
hg19269303
hg18269303
hg17269303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694473
Samples
Known GenesBEGAIN, DLK1, LINC00523, WDR25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521690
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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