A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592171



Internal ID20965242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32375711..32376246hg38UCSC Ensembl
chr13:32949848..32950383hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232672
Samples
Known GenesBRCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592171
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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