A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9251



Internal ID15193516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25265296..25356221hg38UCSC Ensembl
Outerchr1:25591787..25682712hg19UCSC Ensembl
Outerchr1:25464374..25555299hg18UCSC Ensembl
Outerchr1:25337102..25428028hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3890926
hg1990926
hg1890926
hg1790927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7174
Supporting Variants
SamplesNA18517
Known GenesRHD, TMEM50A
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)nssv9251
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