A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428380



Internal ID22486250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162634085..162642364hg38UCSC Ensembl
chr5:162061091..162069370hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg388280
hg198280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428380
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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