A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944926



Internal ID22720398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37798503..37811123hg38UCSC Ensembl
chr18:35378467..35391087hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3812621
hg1912621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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