A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509278



Internal ID22567228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53904951..53906150hg38UCSC Ensembl
chr8:54817511..54818710hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852573
Supporting Variants
Samples
Known GenesRGS20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509278
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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