A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4855



Internal ID15543036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:109254865..109266450hg38UCSC Ensembl
Outerchr5:108590566..108602151hg19UCSC Ensembl
Outerchr5:108618465..108630050hg18UCSC Ensembl
Outerchr5:108618465..108630050hg17UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3811586
hg1911586
hg1811586
hg1711586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4955
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)nssv4855
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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