A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498387



Internal ID22556322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177676171..177682164hg38UCSC Ensembl
chr5:177103172..177109165hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg385994
hg195994
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842487
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498387
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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