A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576965



Internal ID20950036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29201896..29205423hg38UCSC Ensembl
chr13:29776033..29779560hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg383528
hg193528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218682
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576965
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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