A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588048



Internal ID20961119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35073563..35074269hg38UCSC Ensembl
chr17:33400582..33401288hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242136
Samples
Known GenesRAD51L3-RFFL, RFFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588048
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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