A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565136



Internal ID20938207
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 StatusM
Merged Variants
Supporting Variantsnssv18266034
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)nsv6565136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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