A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593545



Internal ID20966616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14222225..14223139hg38UCSC Ensembl
chr12:14375159..14376073hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1425n223
Supporting Variantsnssv18233305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593545
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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