A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4135



Internal ID15548814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:178124769..178169517hg38UCSC Ensembl
Outerchr3:177842557..177887305hg19UCSC Ensembl
Outerchr3:179325251..179369999hg18UCSC Ensembl
Outerchr3:179325259..179370007hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3844749
hg1944749
hg1844749
hg1744749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7898
SamplesNA12156
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)nsv4135
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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