A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9329



Internal ID15193594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13077274..13110766hg38UCSC Ensembl
Outerchr1:13144722..13178238hg19UCSC Ensembl
Outerchr1:13067309..13100825hg18UCSC Ensembl
Outerchr1:12968705..13002221hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3833493
hg1933517
hg1833517
hg1733517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7172
Supporting Variants
SamplesNA18517
Known Genes
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)nssv9329
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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