A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431957



Internal ID22489828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142952385..142953656hg38UCSC Ensembl
chr8:144033802..144035073hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431957
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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