A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413288



Internal ID22471158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174958477..174958561hg38UCSC Ensembl
chr5:174385480..174385564hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887828
Supporting Variants
Samples
Known GenesFLJ16171
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413288
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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