A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591387



Internal ID20964458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30573519..30574225hg38UCSC Ensembl
chr12:30726452..30727158hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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