A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10682



Internal ID15195430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123942311..123993465hg38UCSC Ensembl
Outerchr9:126704590..126755744hg19UCSC Ensembl
Outerchr9:125744411..125795565hg18UCSC Ensembl
Outerchr9:123784144..123835298hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3851155
hg1951155
hg1851155
hg1751155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7435
Supporting Variants
SamplesNA18956
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)nssv10682
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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