A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439



Internal ID15549148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:100019271..100053368hg38UCSC Ensembl
Outerchr4:100940428..100974525hg19UCSC Ensembl
Outerchr4:101159451..101193548hg18UCSC Ensembl
Outerchr4:101297606..101331703hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg385921
hg195921
hg185921
hg175921
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3133
SamplesNA18555
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)nsv4439
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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