A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519608



Internal ID295957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3787042..3791174hg38UCSC Ensembl
chr19:3787040..3791172hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384133
hg194133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720617
Samples
Known GenesMATK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519608
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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