A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4666



Internal ID15196497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:128942534..128957857hg38UCSC Ensembl
Outerchr3:128661377..128676700hg19UCSC Ensembl
Outerchr3:130144067..130159390hg18UCSC Ensembl
Outerchr3:130144075..130159398hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3815324
hg1915324
hg1815324
hg1715324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3996
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)nssv4666
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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