A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579600



Internal ID20952671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73705309..73706136hg38UCSC Ensembl
chr13:74279446..74280273hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227980
Samples
Known GenesKLF12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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