A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381932



Internal ID22439802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40707243..40707552hg38UCSC Ensembl
chr15:40999441..40999750hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934517
Supporting Variants
Samples
Known GenesRAD51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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