A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506112



Internal ID22564057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121054984..121057200hg38UCSC Ensembl
chr8:122067224..122069440hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg382217
hg192217
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506112
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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