A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936834



Internal ID22712194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37819723..37825782hg38UCSC Ensembl
chr18:35399687..35405746hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386060
hg196060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370726
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936834
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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