A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526200



Internal ID15453493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:31839305..31985166hg38UCSC Ensembl
Innerchr14:32308511..32454372hg19UCSC Ensembl
Innerchr14:31378262..31524123hg18UCSC Ensembl
Innerchr14:31378262..31524123hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38145862
hg19145862
hg18145862
hg17145862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702463
Samples
Known GenesNUBPL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526200
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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