A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497386



Internal ID22555320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54709478..54715413hg38UCSC Ensembl
chr5:54005306..54011241hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg385936
hg195936
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843090
Supporting Variants
Samples
Known GenesLOC102467080
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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