A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519976



Internal ID296317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3543485..3543543hg38UCSC Ensembl
chr19:3543483..3543541hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720589
Samples
Known GenesC19orf71, MFSD12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519976
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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