A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509989



Internal ID22567939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80380381..80393381hg38UCSC Ensembl
chr8:81292616..81305616hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3813001
hg1913001
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850066
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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