A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518834



Internal ID20892195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30875755..30883463hg38UCSC Ensembl
chr19:31366662..31374370hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387709
hg197709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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