A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589691



Internal ID21538257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35027950..35034148hg38UCSC Ensembl
chr17:33354969..33361167hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386199
hg196199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091271
SamplesHG02818
Known GenesRAD51L3-RFFL, RFFL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589691
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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