A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10090



Internal ID15196021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:84051706..84061995hg38UCSC Ensembl
Outerchr1:84517389..84527678hg19UCSC Ensembl
Outerchr1:84289977..84300266hg18UCSC Ensembl
Outerchr1:84229410..84239699hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3810290
hg1910290
hg1810290
hg1710290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1732
Supporting Variants
SamplesNA18956
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)nssv10090
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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