A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404490



Internal ID22462360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77781311..77781370hg38UCSC Ensembl
chr18:75493267..75493326hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940158
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404490
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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