A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2642



Internal ID15540469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:41408423..41452895hg38UCSC Ensembl
Outerchr7:41448021..41492493hg19UCSC Ensembl
Outerchr7:41414546..41459018hg18UCSC Ensembl
Outerchr7:41221261..41265733hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3844473
hg1944473
hg1844473
hg1744473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5715
Supporting Variants
SamplesNA18555
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)nssv2642
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