A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524824



Internal ID20898185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58271243..58271947hg38UCSC Ensembl
chr19:58782609..58783313hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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