A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592973



Internal ID20966044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122070339..122070759hg38UCSC Ensembl
chr12:122508245..122508665hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592973
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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