A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445298



Internal ID22503168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54653197..54664348hg38UCSC Ensembl
chr8:55565757..55576908hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3811152
hg1911152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445298
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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