A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522821



Internal ID20896182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51392290..51451683hg38UCSC Ensembl
chr19:51895544..51954937hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3859394
hg1959394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198300
Samples
Known GenesLOC100129083, SIGLEC10, SIGLEC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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