A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508649



Internal ID22566599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21837366..21839738hg38UCSC Ensembl
chr8:21694878..21697250hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508649
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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