A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411088



Internal ID22468958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150463133..150467514hg38UCSC Ensembl
chr5:149842696..149847077hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg384382
hg194382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411088
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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