A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7190



Internal ID15552175
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 StatusM
Merged Variants
Supporting Variantsnssv6181, nssv574
SamplesNA12156, NA19240
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)nsv7190
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer