A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4928



Internal ID15549686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:98354276..98399195hg38UCSC Ensembl
Outerchr5:97689980..97734899hg19UCSC Ensembl
Outerchr5:97717884..97762799hg18UCSC Ensembl
Outerchr5:97717884..97762799hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3844920
hg1944920
hg1844916
hg1744916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8126
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)nsv4928
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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