A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7434



Internal ID15205757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114900117..120805395hg38UCSC Ensembl
Outerchr9:117662397..123567673hg19UCSC Ensembl
Outerchr9:116702218..122607494hg18UCSC Ensembl
Outerchr9:114741951..120647227hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385905279
hg195905277
hg185905277
hg175905277
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5177
SamplesNA19129
Known GenesASTN2, BRINP1, CDK5RAP2, DEC1, FBXW2, LINC00474, LOC100128505, LOC100288842, MEGF9, MIR147A, PAPPA, PAPPA-AS1, SNORA70C, TLR4, TNC, TNFSF8, TRIM32
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)nsv7434
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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