A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497356



Internal ID22555290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52610556..52616334hg38UCSC Ensembl
chr5:51906390..51912168hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg385779
hg195779
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843081
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497356
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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