A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935650



Internal ID22710995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13465823..13466866hg38UCSC Ensembl
chr18:13465822..13466865hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381044
hg191044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376648
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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