A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509977



Internal ID22567927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79957567..79958591hg38UCSC Ensembl
chr8:80869802..80870826hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381025
hg191025
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863310
Supporting Variants
Samples
Known GenesMRPS28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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