A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372377



Internal ID22598046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56354739..56359318hg38UCSC Ensembl
chr18:54021970..54026549hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg384580
hg194580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372377
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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