A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516296



Internal ID20889657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41430132..41433349hg38UCSC Ensembl
chr19:41936037..41939254hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383218
hg193218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048081
Samples
Known GenesATP5SL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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