A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591538



Internal ID20964609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40716683..40717360hg38UCSC Ensembl
chr15:41008881..41009558hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238272
Samples
Known GenesRAD51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591538
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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