A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585956



Internal ID20959027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43747599..43747838hg38UCSC Ensembl
chr12:44141402..44141641hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227894
Samples
Known GenesPUS7L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585956
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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