A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449263



Internal ID22507133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53274043..53274584hg38UCSC Ensembl
chr8:54186603..54187144hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449263
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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