A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388666



Internal ID22446536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36141775..36144104hg38UCSC Ensembl
chr1:36607376..36609705hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382330
hg192330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868275
Supporting Variants
Samples
Known GenesTRAPPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388666
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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