A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534352



Internal ID20907713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37965357..38068076hg38UCSC Ensembl
chr19:38455997..38558716hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg38102720
hg19102720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198094
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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