A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4060



Internal ID15548732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:150187605..150232079hg38UCSC Ensembl
Outerchr3:149905392..149949866hg19UCSC Ensembl
Outerchr3:151388082..151432556hg18UCSC Ensembl
Outerchr3:151388090..151432564hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3844475
hg1944475
hg1844475
hg1744475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2423
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)nsv4060
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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