A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509971



Internal ID22567921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79375863..79379122hg38UCSC Ensembl
chr8:80288098..80291357hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg383260
hg193260
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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