A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3826n223



Internal ID22806794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32866952..42766565hg38UCSC Ensembl
chr2:33092019..42993705hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg389899614
hg199901687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6540167, nsv6539485, nsv6548072, nsv6542757
Samples
Known GenesARHGEF33, ATL2, C2orf91, CDC42EP3, CDKL4, CEBPZ, CEBPZ-AS1, COX7A2L, CRIM1, CYP1B1, CYP1B1-AS1, DHX57, EIF2AK2, EML4, FAM98A, FEZ2, GALM, GEMIN6, GPATCH11, HEATR5B, HNRNPLL, KCNG3, LINC00486, LOC100271832, LOC100288911, LOC375196, LOC388942, LOC728730, LTBP1, MAP4K3, MORN2, MTA3, MYADML, NDUFAF7, OXER1, PKDCC, PRKD3, QPCT, RASGRP3, RMDN2, RMDN2-AS1, SLC8A1, SLC8A1-AS1, SOS1, SRSF7, STRN, SULT6B1, THUMPD2, TMEM178A, VIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3826n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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