A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7055



Internal ID15536809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187417608..187463040hg38UCSC Ensembl
Outerchr3:187135396..187180828hg19UCSC Ensembl
Outerchr3:188618090..188663522hg18UCSC Ensembl
Outerchr3:188618098..188663530hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3845433
hg1945433
hg1845433
hg1745433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7357
Supporting Variants
SamplesNA12156
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)nssv7055
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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