A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932226



Internal ID22707520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35035728..35038214hg38UCSC Ensembl
chr17:33362747..33365233hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382487
hg192487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382838
Samples
Known GenesRAD51L3-RFFL, RFFL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932226
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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