A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504882



Internal ID22562826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107158292..107166782hg38UCSC Ensembl
chr8:108170520..108179010hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg388491
hg198491
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504882
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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