A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406806



Internal ID22464676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76052485..76054136hg38UCSC Ensembl
chr18:73764440..73766091hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406806
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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