A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4857



Internal ID15543033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:114982979..115007944hg38UCSC Ensembl
Outerchr5:114318676..114343641hg19UCSC Ensembl
Outerchr5:114346575..114371540hg18UCSC Ensembl
Outerchr5:114346575..114371540hg17UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3824966
hg1924966
hg1824966
hg1724966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4964
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)nssv4857
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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