A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5087



Internal ID15549861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:156033774..156089188hg38UCSC Ensembl
Outerchr5:155460784..155516198hg19UCSC Ensembl
Outerchr5:155393362..155448776hg18UCSC Ensembl
Outerchr5:155393362..155448776hg17UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3855415
hg1955415
hg1855415
hg1755415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv508, nssv9415, nssv11113, nssv9678
SamplesNA18507, NA15510, NA18517, NA19240
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)nsv5087
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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