A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2867



Internal ID15195007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:19055764..19076114hg38UCSC Ensembl
Outerchr1:19382258..19402608hg19UCSC Ensembl
Outerchr1:19254845..19275195hg18UCSC Ensembl
Outerchr1:19127564..19147914hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg385892
hg195892
hg185892
hg175892
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5298
Supporting Variants
SamplesNA18555
Known GenesUBR4
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)nssv2867
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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