A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506876



Internal ID22564824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131551199..131571735hg38UCSC Ensembl
chr8:132563446..132583982hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3820537
hg1920537
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506876
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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