A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940752



Internal ID22716165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9646090..9646695hg38UCSC Ensembl
chr18:9646088..9646693hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940752
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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