A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955



Internal ID15550816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:133312162..133323781hg38UCSC Ensembl
Outerchr7:132996916..133008535hg19UCSC Ensembl
Outerchr7:132647456..132659075hg18UCSC Ensembl
Outerchr7:132454171..132465790hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3811620
hg1911620
hg1811620
hg1711620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8430
SamplesNA12156
Known GenesEXOC4
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)nsv5955
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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