A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372378



Internal ID22598047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11877198..11880002hg38UCSC Ensembl
chr18:11877197..11880001hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382805
hg192805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944846
Supporting Variants
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372378
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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