A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575170



Internal ID20948241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:274842..1630767hg38UCSC Ensembl
chr5:274957..1630882hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381355926
hg191355926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5585n223
Supporting Variantsnssv18269547
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)nsv6575170
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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