A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11158



Internal ID15539421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:109786887..109821875hg38UCSC Ensembl
Outerchr7:109426944..109461932hg19UCSC Ensembl
Outerchr7:109214180..109249168hg18UCSC Ensembl
Outerchr7:109020895..109055883hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3834989
hg1934989
hg1834989
hg1734989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5896
Supporting Variants
SamplesNA15510
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)nssv11158
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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