A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524451



Internal ID20897812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41433952..41442055hg38UCSC Ensembl
chr19:41939857..41947960hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg388104
hg198104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048082
Samples
Known GenesATP5SL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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