A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350609



Internal ID22576278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167375782..167375886hg38UCSC Ensembl
chr1:167345019..167345123hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882570
Supporting Variants
Samples
Known GenesPOU2F1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350609
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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