A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241991



Internal ID20809031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75735470..77868880hg38UCSC Ensembl
chr15:76027811..78161222hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382133411
hg192133412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587760
Supporting Variants
Samples
Known GenesC15orf27, DNM1P35, ETFA, FBXO22, FBXO22-AS1, HMG20A, ISL2, LINC00597, LINGO1, LOC253044, MIR4313, NRG4, PEAK1, PSTPIP1, RCN2, SCAPER, TSPAN3, TYRO3P, UBE2Q2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.05605


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