A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432312



Internal ID22490182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97742365..97742507hg38UCSC Ensembl
chr8:98754593..98754735hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432312
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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