A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531782



Internal ID20905143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31170121..31170695hg38UCSC Ensembl
chr19:31661027..31661601hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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