A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7426



Internal ID15552434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62872669..62915313hg38UCSC Ensembl
Outerchr9:66528493..66571137hg19UCSC Ensembl
Outerchr9:66268313..66310957hg18UCSC Ensembl
Outerchr9:64209765..64252409hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3842645
hg1942645
hg1842645
hg1742645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806
SamplesNA19240
Known GenesMGC21881
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)nsv7426
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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