A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582027



Internal ID20955098
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 StatusM
Merged Variants
Supporting Variantsnssv18232796
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)nsv6582027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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