A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178067



Internal ID20745107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51964071..52025722hg38UCSC Ensembl
chr15:52256268..52317919hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3861652
hg1961652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497327
Supporting Variants
Samples
Known GenesLEO1, MAPK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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