A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581952



Internal ID20955023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85024593..85025236hg38UCSC Ensembl
chr12:85418371..85419014hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233804
Samples
Known GenesTSPAN19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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