A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592763



Internal ID20965834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41301494..41302320hg38UCSC Ensembl
chr13:41875630..41876456hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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