A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4140



Internal ID15202134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:179666173..179711916hg38UCSC Ensembl
Outerchr3:179383961..179429704hg19UCSC Ensembl
Outerchr3:180866655..180912398hg18UCSC Ensembl
Outerchr3:180866663..180912406hg17UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3845744
hg1945744
hg1845744
hg1745744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7053
SamplesNA12156
Known GenesUSP13
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)nsv4140
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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