A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767



Internal ID15549509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:24914374..24959306hg38UCSC Ensembl
Outerchr5:24914483..24959415hg19UCSC Ensembl
Outerchr5:24950240..24995172hg18UCSC Ensembl
Outerchr5:24950240..24995172hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3844933
hg1944933
hg1844933
hg1744933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8081
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)nsv4767
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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