A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116463



Internal ID18913956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75332346..77948110hg38UCSC Ensembl
Outerchr15:75624687..78240452hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382615765
hg192615766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978644
SamplesKWS2
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
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116463
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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