A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2584n223



Internal ID22805552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75332358..77948110hg38UCSC Ensembl
chr15:75624699..78240452hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382615753
hg192615754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6595525, nsv6579607, nsv6578620, nsv6582103, nsv6577891, nsv6579140, nsv6587760
Samples
Known GenesC15orf27, COMMD4, CSPG4, DNM1P35, ETFA, FBXO22, FBXO22-AS1, HMG20A, IMP3, ISL2, LINC00597, LINGO1, LOC253044, LOC645752, MAN2C1, MIR4313, MIR631, NEIL1, NRG4, ODF3L1, PEAK1, PSTPIP1, PTPN9, RCN2, SCAPER, SIN3A, SNUPN, SNX33, TSPAN3, TYRO3P, UBE2Q2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2584n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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