A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9305



Internal ID15540256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20406055..22290807hg38UCSC Ensembl
Outerchr15:20611308..22578758hg19UCSC Ensembl
Outerchr15:18871322..20080122hg18UCSC Ensembl
Outerchr15:18871322..20080122hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381884753
hg191967451
hg181208801
hg171208801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA18517
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)nssv9305
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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