A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231284



Internal ID20798324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118910158..125783778hg38UCSC Ensembl
chr10:120669670..127472347hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg386873621
hg196802678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585886
Supporting Variants
Samples
Known GenesACADSB, ARMS2, ATE1, BAG3, BTBD16, BUB3, C10orf120, C10orf137, C10orf85, C10orf88, CHST15, CPXM2, CTBP2, CUZD1, DMBT1, EIF3A, FAM175B, FAM24A, FAM24B, FAM24B-CUZD1, FAM45A, FAM45B, FAM53B, FGFR2, FLJ37035, FLJ46361, GPR26, GRK5, HMX2, HMX3, HTRA1, IKZF5, INPP5F, LHPP, LOC100169752, LOC283038, LOC399815, MCMBP, METTL10, MIR3941, MIR4296, MIR4681, MIR4682, MIR5694, MMP21, NANOS1, NKX1-2, NSMCE4A, OAT, PLEKHA1, PPAPDC1A, PRDX3, PSTK, RGS10, SEC23IP, SFXN4, SNORA19, TACC2, TEX36, TIAL1, WDR11, WDR11-AS1, ZRANB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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