A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4280



Internal ID15548974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:27123187..27168228hg38UCSC Ensembl
Outerchr4:27124809..27169850hg19UCSC Ensembl
Outerchr4:26733907..26778948hg18UCSC Ensembl
Outerchr4:26801078..26846119hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3845042
hg1945042
hg1845042
hg1745042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7940
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)nsv4280
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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