A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2097



Internal ID15541380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20392856..22297596hg38UCSC Ensembl
Outerchr15:20598109..22585547hg19UCSC Ensembl
Outerchr15:18858123..20086911hg18UCSC Ensembl
Outerchr15:18858123..20086911hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381904741
hg191987439
hg181228789
hg171228789
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA18555
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)nssv2097
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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