A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510094



Internal ID22568044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85016597..85019584hg38UCSC Ensembl
chr8:85928832..85931819hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg382988
hg192988
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510094
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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