A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499913



Internal ID22557849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67759341..67781704hg38UCSC Ensembl
chr5:67055169..67077532hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3822364
hg1922364
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843397
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499913
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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