A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355563



Internal ID22581232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151763145..151763324hg38UCSC Ensembl
chr1:151735621..151735800hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874811
Supporting Variants
Samples
Known GenesMRPL9, OAZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355563
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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