A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521372



Internal ID15448665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39998545..40123176hg38UCSC Ensembl
Innerchr14:40467749..40592380hg19UCSC Ensembl
Innerchr14:39537500..39662131hg18UCSC Ensembl
Innerchr14:39537500..39662131hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38124632
hg19124632
hg18124632
hg17124632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697981
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521372
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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