A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7433



Internal ID15552442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114584334..114620106hg38UCSC Ensembl
Outerchr9:117346614..117382386hg19UCSC Ensembl
Outerchr9:116386435..116422207hg18UCSC Ensembl
Outerchr9:114426168..114461940hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3835773
hg1935773
hg1835773
hg1735773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6293
SamplesNA12156
Known GenesATP6V1G1, C9orf91
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)nsv7433
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer