A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9432



Internal ID15193697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:248446791..248602246hg38UCSC Ensembl
Outerchr1:248610092..248765547hg19UCSC Ensembl
Outerchr1:246676715..246832170hg18UCSC Ensembl
Outerchr1:244936133..245091588hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38155456
hg19155456
hg18155456
hg17155456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7193
Supporting Variants
SamplesNA18517
Known GenesOR2G6, OR2T10, OR2T2, OR2T29, OR2T3, OR2T34, OR2T5
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)nssv9432
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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