A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516032



Internal ID20889393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49333001..49334800hg38UCSC Ensembl
chr19:49836258..49838057hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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