A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524398



Internal ID20897759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3088847..3090395hg38UCSC Ensembl
chr19:3088845..3090393hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381549
hg191549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524398
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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