A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485200



Internal ID22543111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142131184..142133683hg38UCSC Ensembl
chr3:141850026..141852525hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834689
Supporting Variants
Samples
Known GenesTFDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485200
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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