A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509688



Internal ID22567638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65432613..65438599hg38UCSC Ensembl
chr8:66344848..66350834hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385987
hg195987
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509688
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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