A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416590



Internal ID22474460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2269553..2271242hg38UCSC Ensembl
chr5:2269667..2271356hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416590
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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