A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4557



Internal ID15549278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:153637869..153682908hg38UCSC Ensembl
Outerchr4:154559021..154604060hg19UCSC Ensembl
Outerchr4:154778471..154823510hg18UCSC Ensembl
Outerchr4:154916626..154961665hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3845040
hg1945040
hg1845040
hg1745040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2487
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)nsv4557
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