A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586261



Internal ID20959332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88348743..88349567hg38UCSC Ensembl
chr13:89000998..89001822hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586261
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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