A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491309



Internal ID22549234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182546606..182548930hg38UCSC Ensembl
chr4:183467759..183470083hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382325
hg192325
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838480
Supporting Variants
Samples
Known GenesTENM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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