A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592240



Internal ID20965311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:123687528..123688357hg38UCSC Ensembl
chr12:124172075..124172904hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223016
Samples
Known GenesTCTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592240
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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