A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266034



Internal ID20833074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74413523..83001891hg38UCSC Ensembl
chr4:75279240..83923044hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg388588369
hg198643805
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565136
Supporting Variants
Samples
Known GenesANTXR2, ANXA3, AREG, ART3, BMP2K, BMP3, BTC, C4orf22, C4orf26, CCDC158, CCNG2, CCNI, CDKL2, CNOT6L, CXCL10, CXCL11, CXCL13, CXCL9, ENOPH1, FAM47E, FAM47E-STBD1, FGF5, FRAS1, G3BP2, GK2, HNRNPD, HNRNPDL, LIN54, LINC00575, LINC00989, LINC01088, LINC01094, LOC441025, MIR4450, MIR575, MRPL1, NAA11, NAAA, NUP54, PAQR3, PARM1, PCAT4, PPEF2, PRDM8, PRKG2, RASGEF1B, RCHY1, SCARB2, SCD5, SDAD1, SEC31A, SEPT11, SHROOM3, SOWAHB, STBD1, THAP6, THAP9, THAP9-AS1, TMEM150C, USO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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