A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269559



Internal ID20836599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:283666..1620804hg38UCSC Ensembl
chr5:283781..1620919hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381337139
hg191337139
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563131
Supporting Variants
Samples
Known GenesAHRR, BRD9, C5orf55, CEP72, CLPTM1L, EXOC3, LOC100506688, LOC100996325, LOC728613, LPCAT1, MIR4456, MIR4457, MIR4635, MIR6075, NKD2, PDCD6, PP7080, SDHAP3, SLC12A7, SLC6A18, SLC6A19, SLC6A3, SLC9A3, TERT, TPPP, TRIP13, ZDHHC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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