A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498384



Internal ID22556319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177645073..177669655hg38UCSC Ensembl
chr5:177072074..177096656hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3824583
hg1924583
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841622
Supporting Variants
Samples
Known GenesLOC202181
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498384
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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