A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577778



Internal ID20950849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95305602..95306841hg38UCSC Ensembl
chr12:95699378..95700617hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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