A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498079



Internal ID22556013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6757950..6759449hg38UCSC Ensembl
chr5:6758063..6759562hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498079
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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