A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107315



Internal ID22016548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:276886..1627022hg38UCSC Ensembl
chr5:277001..1627137hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381350137
hg191350137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554902
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
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107315
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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