A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4861



Internal ID15543026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:6678148..6698392hg38UCSC Ensembl
Outerchr1:6738208..6758452hg19UCSC Ensembl
Outerchr1:6660795..6681039hg18UCSC Ensembl
Outerchr1:6672474..6692718hg17UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg388170
hg198170
hg188170
hg178170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1298
Supporting Variants
SamplesNA19129
Known GenesDNAJC11
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)nssv4861
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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