A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7235



Internal ID15552224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:108083148..108119606hg38UCSC Ensembl
Outerchr12:108476925..108513383hg19UCSC Ensembl
Outerchr12:107001055..107037513hg18UCSC Ensembl
Outerchr12:106979392..107015850hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3836459
hg1936459
hg1836459
hg1736459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5451, nssv9288
SamplesNA18517, NA19129
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)nsv7235
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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