A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517665



Internal ID20891026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14212414..14214647hg38UCSC Ensembl
chr19:14323226..14325459hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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