A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585904



Internal ID20958975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119639336..119640456hg38UCSC Ensembl
chr12:120077141..120078261hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222173
Samples
Known GenesTMEM233
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585904
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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