A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583855



Internal ID20956926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64523124..64524139hg38UCSC Ensembl
chr12:64916904..64917919hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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