A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445343



Internal ID22503213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104704159..104704311hg38UCSC Ensembl
chr8:105716387..105716539hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927287
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445343
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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