A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525074



Internal ID20898435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10267466..10268876hg38UCSC Ensembl
chr19:10378142..10379552hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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