A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435543



Internal ID22493413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137061045..137070274hg38UCSC Ensembl
chr8:138073288..138082517hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg389230
hg199230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435543
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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