A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937909



Internal ID22713283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59834847..59836575hg38UCSC Ensembl
chr18:57502079..57503807hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg381729
hg191729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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