A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582103



Internal ID20955174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75332358..77947953hg38UCSC Ensembl
chr15:75624699..78240295hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382615596
hg192615597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2584n223
Supporting Variantsnssv18241966
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)nsv6582103
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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