A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9387



Internal ID15540338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187422358..187459705hg38UCSC Ensembl
Outerchr3:187140146..187177493hg19UCSC Ensembl
Outerchr3:188622840..188660187hg18UCSC Ensembl
Outerchr3:188622848..188660195hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3837348
hg1937348
hg1837348
hg1737348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7357
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)nssv9387
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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