A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4278



Internal ID15202285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:26196205..26225504hg38UCSC Ensembl
Outerchr4:26197827..26227126hg19UCSC Ensembl
Outerchr4:25806925..25836224hg18UCSC Ensembl
Outerchr4:25874096..25903395hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388690
hg198690
hg188690
hg178690
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv379
SamplesNA19240
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)nsv4278
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer