A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589252



Internal ID20962323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92745376..92748342hg38UCSC Ensembl
chr12:93139152..93142118hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382967
hg192967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237092
Samples
Known GenesPLEKHG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589252
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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