A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11166



Internal ID15539413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143731946..143849140hg38UCSC Ensembl
Outerchr7:143429039..143546233hg19UCSC Ensembl
Outerchr7:143059972..143177166hg18UCSC Ensembl
Outerchr7:142866687..142983881hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38117195
hg19117195
hg18117195
hg17117195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7408
Supporting Variants
SamplesNA15510
Known GenesCTAGE6, LOC154761
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)nssv11166
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