A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383603



Internal ID22441473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36408056..36421762hg38UCSC Ensembl
chr18:33988019..34001725hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3813707
hg1913707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941800
Supporting Variants
Samples
Known GenesFHOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383603
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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