A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579316



Internal ID20952387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80355809..82694011hg38UCSC Ensembl
chr15:80648151..83362763hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382338203
hg192714613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239767
Samples
Known GenesABHD17C, ADAMTS7P1, AP3B2, ARNT2, C15orf26, CPEB1, CSPG4P8, EFTUD1, FAM154B, GOLGA6L10, GOLGA6L20, GOLGA6L9, IL16, KIAA1199, LOC283692, LOC727751, LOC80154, MESDC1, MESDC2, MEX3B, MIR4514, MIR549, RPS17, RPS17L, STARD5, TMC3, UBE2Q2P2, UBE2Q2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579316
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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