A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4706



Internal ID15542979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:188956314..189001460hg38UCSC Ensembl
Outerchr3:188674103..188719249hg19UCSC Ensembl
Outerchr3:190156797..190201943hg18UCSC Ensembl
Outerchr3:190156805..190201951hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3845147
hg1945147
hg1845147
hg1745147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4163
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)nssv4706
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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