A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576953



Internal ID20950024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64733298..66057590hg38UCSC Ensembl
chr12:65127078..66451370hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg381324293
hg191324293
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1568n223
Supporting Variantsnssv18234159
Samples
Known GenesFLJ41278, GNS, HMGA2, LEMD3, MIR6074, MSRB3, RPSAP52, TBC1D30, WIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576953
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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