A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514964



Internal ID20888319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98985601..98992800hg38UCSC Ensembl
chr14:99451938..99459137hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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