A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498104



Internal ID22556038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69370761..69373328hg38UCSC Ensembl
chr5:68666588..68669155hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg382568
hg192568
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843469
Supporting Variants
Samples
Known GenesRAD17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498104
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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