A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584449



Internal ID20957520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66057683..75201071hg38UCSC Ensembl
chr12:66451463..75594851hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg389143389
hg199143389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1578n223
Supporting Variantsnssv18233631
Samples
Known GenesATXN7L3B, BEST3, CAND1, CCT2, CNOT2, CPM, CPSF6, DYRK2, FRS2, GRIP1, HELB, IFNG, IFNG-AS1, IL22, IL26, IRAK3, KCNC2, KCNMB4, LGR5, LLPH, LOC100130075, LOC100507175, LOC100507250, LOC100507377, LRRC10, LYZ, MDM1, MDM2, MIR1279, MIR3913-1, MIR3913-2, MRS2P2, NUP107, PTPRB, PTPRR, RAB21, RAB3IP, RAP1B, SLC35E3, SNORA70G, TBC1D15, THAP2, TMBIM4, TMEM19, TPH2, TRHDE, TRHDE-AS1, TSPAN8, YEATS4, ZFC3H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584449
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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