A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4796



Internal ID15549541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:38036066..38080418hg38UCSC Ensembl
Outerchr5:38036168..38080520hg19UCSC Ensembl
Outerchr5:38071925..38116277hg18UCSC Ensembl
Outerchr5:38071925..38116277hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3844353
hg1944353
hg1844353
hg1744353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2518
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)nsv4796
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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