A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5107



Internal ID15549883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:165054595..165088534hg38UCSC Ensembl
Outerchr5:164481601..164515540hg19UCSC Ensembl
Outerchr5:164414179..164448118hg18UCSC Ensembl
Outerchr5:164414179..164448118hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385499
hg195499
hg185499
hg175499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8182
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)nsv5107
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