A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4282



Internal ID15548976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:27913033..27957852hg38UCSC Ensembl
Outerchr4:27914655..27959474hg19UCSC Ensembl
Outerchr4:27523753..27568572hg18UCSC Ensembl
Outerchr4:27590924..27635743hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3844820
hg1944820
hg1844820
hg1744820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7941
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)nsv4282
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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