A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508755



Internal ID22566705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28591489..28595663hg38UCSC Ensembl
chr8:28449006..28453180hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg384175
hg194175
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861146
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508755
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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