A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262707



Internal ID20829747
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 StatusS
Merged Variantsnsv6537526
Supporting Variants
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)nssv18262707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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