A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411147



Internal ID22469017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:144591911..144599538hg38UCSC Ensembl
chr5:143971474..143979101hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg387628
hg197628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411147
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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