A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10922



Internal ID15539510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20245320..21069766hg38UCSC Ensembl
Outerchr15:20450573..21275095hg19UCSC Ensembl
Outerchr15:18710587..19539754hg18UCSC Ensembl
Outerchr15:18710587..19539754hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38824447
hg19824523
hg18829168
hg17829168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA15510
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
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)nssv10922
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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