A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537526



Internal ID20910860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94859299..102665887hg38UCSC Ensembl
chr3:94578143..102384731hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg387806589
hg197806589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262707
Samples
Known GenesABI3BP, ARL6, CEP97, CLDND1, CMSS1, COL8A1, CPOX, CRYBG3, DCBLD2, EPHA6, FAM172BP, FILIP1L, GABRR3, GPR128, GPR15, IMPG2, LINC00879, LNP1, LOC152225, MINA, MIR3921, MIR548G, MIR8060, MTHFD2P1, NFKBIZ, NIT2, NXPE3, OR5AC2, OR5H1, OR5H14, OR5H15, OR5H2, OR5H6, OR5K1, OR5K2, OR5K3, OR5K4, PCNP, PDCL3P4, RPL24, SENP7, ST3GAL6, ST3GAL6-AS1, TBC1D23, TFG, TMEM30C, TMEM45A, TOMM70A, TRMT10C, ZBTB11, ZBTB11-AS1, ZPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537526
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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