A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577166



Internal ID20950237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73067968..73068705hg38UCSC Ensembl
chr13:73642106..73642843hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1915n223
Supporting Variantsnssv18219865
Samples
Known GenesKLF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577166
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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