A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594294



Internal ID20967365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102832983..102833620hg38UCSC Ensembl
chr13:103485333..103485970hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218107
Samples
Known GenesBIVM, BIVM-ERCC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594294
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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