A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231076



Internal ID20798116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66057683..75778623hg38UCSC Ensembl
chr12:66451463..76172403hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg389720941
hg199720941
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582770
Supporting Variants
Samples
Known GenesATXN7L3B, BEST3, CAND1, CAPS2, CCT2, CNOT2, CPM, CPSF6, DYRK2, FRS2, GLIPR1, GLIPR1L1, GLIPR1L2, GRIP1, HELB, IFNG, IFNG-AS1, IL22, IL26, IRAK3, KCNC2, KCNMB4, KRR1, 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)nssv18231076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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