A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588794



Internal ID20961865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:63710892..66057683hg38UCSC Ensembl
chr12:64104672..66451463hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg382346792
hg192346792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1557n223
Supporting Variantsnssv18229326
Samples
Known GenesC12orf56, C12orf66, FLJ41278, GNS, HMGA2, LEMD3, MIR548C, MIR548Z, MIR6074, MSRB3, RASSF3, RPSAP52, SRGAP1, TBC1D30, TBK1, TMEM5, WIF1, XPOT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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