A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7703



Internal ID15206053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:20632781..20680091hg38UCSC Ensembl
Outerchr11:20654327..20701637hg19UCSC Ensembl
Outerchr11:20610903..20658213hg18UCSC Ensembl
Outerchr11:20610903..20658213hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3847311
hg1947311
hg1847311
hg1747311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1928, nssv8888
SamplesNA12156, NA18555
Known GenesNELL1, SLC6A5
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)nsv7703
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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