A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4584



Internal ID15202622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:163091996..163125621hg38UCSC Ensembl
Outerchr4:164013148..164046773hg19UCSC Ensembl
Outerchr4:164232598..164266223hg18UCSC Ensembl
Outerchr4:164370753..164404378hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg385644
hg195644
hg185644
hg175644
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4793
SamplesNA19129
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)nsv4584
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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