A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4562



Internal ID15549284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155469318..155513807hg38UCSC Ensembl
Outerchr4:156390470..156434959hg19UCSC Ensembl
Outerchr4:156609920..156654409hg18UCSC Ensembl
Outerchr4:156748075..156792564hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3844490
hg1944490
hg1844490
hg1744490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4674
SamplesNA19129
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)nsv4562
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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