A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524434



Internal ID20897795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21554660..21557800hg38UCSC Ensembl
chr19:21737462..21740602hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg383141
hg193141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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