A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4854



Internal ID15549605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:18546437..18592087hg38UCSC Ensembl
Outerchr1:18872931..18918581hg19UCSC Ensembl
Outerchr1:18745518..18791168hg18UCSC Ensembl
Outerchr1:18618237..18663887hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3845651
hg1945651
hg1845651
hg1745651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6404
SamplesNA12156
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)nsv4854
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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