A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930866



Internal ID22706140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56127583..56132569hg38UCSC Ensembl
chr19:56638952..56643938hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg384987
hg194987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930866
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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