A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583638



Internal ID20956709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30347746..30348181hg38UCSC Ensembl
chr13:30921883..30922318hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230822
Samples
Known GenesLINC00426
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583638
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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