A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4091



Internal ID15202080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:161300752..161346087hg38UCSC Ensembl
Outerchr3:161018540..161063875hg19UCSC Ensembl
Outerchr3:162501234..162546569hg18UCSC Ensembl
Outerchr3:162501242..162546577hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3845336
hg1945336
hg1845336
hg1745336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7046
SamplesNA12156
Known GenesSPTSSB
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)nsv4091
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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