A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv574



Internal ID15545329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:227465615..227496799hg38UCSC Ensembl
Outerchr1:227653316..227684500hg19UCSC Ensembl
Outerchr1:225719939..225751123hg18UCSC Ensembl
Outerchr1:223960051..223991235hg17UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3831185
hg1931185
hg1831185
hg1731185
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7190
Supporting Variants
SamplesNA19240
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)nssv574
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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