A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525481



Internal ID301640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10558957..10559257hg38UCSC Ensembl
chr19:10669633..10669933hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721333
Samples
Known GenesKRI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525481
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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