A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593136



Internal ID20966207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20891679..20892169hg38UCSC Ensembl
chr13:21465818..21466308hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227251
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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