A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4826



Internal ID15543088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:26778294..26804923hg38UCSC Ensembl
Outerchr5:26778403..26805032hg19UCSC Ensembl
Outerchr5:26814160..26840789hg18UCSC Ensembl
Outerchr5:26814160..26840789hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3826630
hg1926630
hg1826630
hg1726630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4768
Supporting Variants
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)nssv4826
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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