A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478917



Internal ID21136470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56945148..56951859hg38UCSC Ensembl
chr14:57411866..57418577hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg386712
hg196712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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