A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581179



Internal ID20954250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114707310..114707765hg38UCSC Ensembl
chr12:115145115..115145570hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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