A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768



Internal ID15549510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:26761581..26810190hg38UCSC Ensembl
Outerchr5:26761690..26810299hg19UCSC Ensembl
Outerchr5:26797447..26846056hg18UCSC Ensembl
Outerchr5:26797447..26846056hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3848610
hg1948610
hg1848610
hg1748610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5988, nssv3338, nssv4826
SamplesNA12156, NA12878, NA19129
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)nsv4768
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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