A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7423



Internal ID15552431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42591225..42693519hg38UCSC Ensembl
Outerchr9:44277600..44379894hg19UCSC Ensembl
Outerchr9:44217596..44319890hg18UCSC Ensembl
Outerchr9:43428673..43530967hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38102295
hg19102295
hg18102295
hg17102295
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803, nssv9765, nssv10660, nssv3717, nssv9764, nssv802
SamplesNA18507, NA12878, NA18956, NA19240
Known Genes
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)nsv7423
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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