A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535420



Internal ID20908781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18977054..18981706hg38UCSC Ensembl
chr19:19087863..19092515hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384653
hg194653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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