A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514998



Internal ID20888354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100370652..100372939hg38UCSC Ensembl
chr14:100836989..100839276hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382288
hg192288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016459
Samples
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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