A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232796



Internal ID20799837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26903422..36846484hg38UCSC Ensembl
chr10:27192351..37135412hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg389943063
hg199943062
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582027
Supporting Variants
Samples
Known GenesACBD5, ANKRD26, ARHGAP12, ARMC4, BAMBI, C10orf126, CCDC7, CCNY, CREM, CUL2, EPC1, FZD8, GJD4, ITGB1, KIAA1462, KIF5B, LINC00202-1, LINC00837, LINC00838, LOC102031319, LRRC37A6P, LYZL1, LYZL2, MAP3K8, MASTL, MIR4683, MIR5586, MIR604, MIR7162, MIR8086, MIR938, MKX, MPP7, MTPAP, NRP1, PARD3, PARD3-AS1, PTCHD3, PTCHD3P1, RAB18, SVIL, SVILP1, WAC, WAC-AS1, YME1L1, ZEB1, ZEB1-AS1, ZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232796
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00057


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