A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110189



Internal ID22019422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143243347..143843862hg38UCSC Ensembl
chr8:144325517..144926034hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38600516
hg19600518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585599
Samples
Known GenesBREA2, CCDC166, EEF1D, FAM83H, FAM83H-AS1, GLI4, GSDMD, MAFA, MAPK15, MIR4664, MIR6845, MIR937, MROH6, NAPRT1, NRBP2, PUF60, PYCRL, RHPN1, RHPN1-AS1, SCRIB, TIGD5, TOP1MT, TSTA3, ZC3H3, ZFP41, ZNF623, ZNF696, ZNF707
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110189
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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