A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489490



Internal ID21147043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20932145..20958230hg38UCSC Ensembl
chr14:21400304..21426389hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3826086
hg1926086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016628
Samples
Known GenesRNASE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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