A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506893



Internal ID22564841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132561021..132570100hg38UCSC Ensembl
chr8:133573268..133582348hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg389080
hg199081
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865999
Supporting Variants
Samples
Known GenesHPYR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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