A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148560



Internal ID18852642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28147412..30831723hg38UCSC Ensembl
Outerchr15:28392558..31123926hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382684312
hg192731369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000598
SamplesKWB1
Known GenesAPBA2, ARHGAP11B, CHRFAM7A, DKFZP434L187, FAM189A1, GOLGA6L7P, GOLGA8F, GOLGA8G, GOLGA8H, GOLGA8J, GOLGA8M, GOLGA8T, HERC2, HERC2P10, HERC2P9, LOC100288637, LOC100289656, LOC101059918, LOC646278, MIR4509-1, MIR4509-2, MIR4509-3, NDNL2, TJP1, ULK4P1, ULK4P2, ULK4P3, WHAMMP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148560
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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