A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705037



Internal ID21377313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231167320..231167625hg38UCSC Ensembl
chr1:231303066..231303371hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389469
Supporting Variants
Samples
Known GenesTRIM67
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705037
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.267241


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