A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6296



Internal ID15190882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123937737..123989616hg38UCSC Ensembl
Outerchr9:126700016..126751895hg19UCSC Ensembl
Outerchr9:125739837..125791716hg18UCSC Ensembl
Outerchr9:123779570..123831449hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3851880
hg1951880
hg1851880
hg1751880
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7435
Supporting Variants
SamplesNA12156
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)nssv6296
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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