A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406804



Internal ID22464674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74172650..74172747hg38UCSC Ensembl
chr18:71839885..71839982hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927776
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406804
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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