A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10620



Internal ID15195492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:248492795..248591869hg38UCSC Ensembl
Outerchr1:248656096..248755170hg19UCSC Ensembl
Outerchr1:246722719..246821793hg18UCSC Ensembl
Outerchr1:244982137..245081211hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3899075
hg1999075
hg1899075
hg1799075
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7193
Supporting Variants
SamplesNA18956
Known GenesOR2G6, OR2T29, OR2T34
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)nssv10620
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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