A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526395



Internal ID20899756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41468543..41524890hg38UCSC Ensembl
chr19:41974448..42031250hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3856348
hg1956803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198813
Samples
Known GenesLOC100505495
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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