A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447653



Internal ID22505523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97620092..97627892hg38UCSC Ensembl
chr8:98632320..98640120hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg387801
hg197801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447653
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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