A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521387



Internal ID297683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57171949..57172203hg38UCSC Ensembl
chr19:57683317..57683571hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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