A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10573



Internal ID15542225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107419645..107463822hg38UCSC Ensembl
Outerchr7:107060090..107104267hg19UCSC Ensembl
Outerchr7:106847326..106891503hg18UCSC Ensembl
Outerchr7:106654041..106698218hg17UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3844178
hg1944178
hg1844178
hg1744178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7404
Supporting Variants
SamplesNA18956
Known GenesCOG5
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)nssv10573
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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