A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500424



Internal ID22558361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89497135..89499834hg38UCSC Ensembl
chr5:88792952..88795651hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500424
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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