A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427971



Internal ID22485841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16973122..16973474hg38UCSC Ensembl
chr5:16973231..16973583hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427971
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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