A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901421



Internal ID1758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36242639..36256370hg38UCSC Ensembl
chr1:36708240..36721971hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3813732
hg1913732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420280
Supporting Variants
Samples
Known GenesTHRAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901421
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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