A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10924



Internal ID15539512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20391031..22298208hg38UCSC Ensembl
Outerchr15:20596284..22586159hg19UCSC Ensembl
Outerchr15:18856298..20087523hg18UCSC Ensembl
Outerchr15:18856298..20087523hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381907178
hg191989876
hg181231226
hg171231226
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA15510
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv10924
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer