A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410173



Internal ID22468043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184099468..184101466hg38UCSC Ensembl
chr3:183817256..183819254hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381999
hg191999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900726
Supporting Variants
Samples
Known GenesHTR3E
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410173
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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