A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517538



Internal ID20890899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2364956..2366308hg38UCSC Ensembl
chr19:2364954..2366306hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381353
hg191353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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