A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4456



Internal ID15549167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:107588133..107632889hg38UCSC Ensembl
Outerchr4:108509290..108554045hg19UCSC Ensembl
Outerchr4:108728739..108773494hg18UCSC Ensembl
Outerchr4:108866894..108911649hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3844757
hg1944756
hg1844756
hg1744756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4774
SamplesNA19129
Known GenesPAPSS1
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)nsv4456
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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