A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517372



Internal ID20890733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40013401..40014900hg38UCSC Ensembl
chr19:40519308..40520807hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047918
Samples
Known GenesZNF546
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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