A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494867



Internal ID22552799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130742917..130753671hg38UCSC Ensembl
chr5:130078610..130089364hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3810755
hg1910755
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494867
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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