A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437781



Internal ID22495651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81050354..81050423hg38UCSC Ensembl
chr8:81962589..81962658hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915217
Supporting Variants
Samples
Known GenesPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437781
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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