A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221435



Internal ID20788475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104070004..110020477hg38UCSC Ensembl
chr11:103940732..109891203hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385950474
hg195950472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578547
Supporting Variants
Samples
Known GenesAASDHPPT, ACAT1, ALKBH8, ATM, C11orf65, C11orf87, CARD16, CARD17, CARD18, CASP1, CASP12, CASP4, CASP5, CUL5, CWF19L2, DDX10, ELMOD1, EXPH5, GRIA4, GUCY1A2, KBTBD3, KDELC2, LOC643733, LOC643923, MSANTD4, NPAT, PDGFD, RAB39A, SLC35F2, SLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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