A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6489



Internal ID15537374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26640932..26685717hg38UCSC Ensembl
Outerchr1:26967423..27012208hg19UCSC Ensembl
Outerchr1:26840010..26884795hg18UCSC Ensembl
Outerchr1:26651565..26696350hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3844786
hg1944786
hg1844786
hg1744786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7175
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)nssv6489
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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