A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9304



Internal ID15540255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20245215..21067932hg38UCSC Ensembl
Outerchr15:20450468..21273261hg19UCSC Ensembl
Outerchr15:18710482..19537920hg18UCSC Ensembl
Outerchr15:18710482..19537920hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38822718
hg19822794
hg18827439
hg17827439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA18517
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)nssv9304
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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