A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425431



Internal ID22483301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160676218..160681452hg38UCSC Ensembl
chr3:160394006..160399240hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385235
hg195235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897053
Supporting Variants
Samples
Known GenesARL14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425431
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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