A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3968



Internal ID15201944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:120347607..120392616hg38UCSC Ensembl
Outerchr3:120066454..120111463hg19UCSC Ensembl
Outerchr3:121549144..121594153hg18UCSC Ensembl
Outerchr3:121549144..121594153hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3845010
hg1945010
hg1845010
hg1745010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7854
SamplesNA12156
Known GenesLRRC58
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)nsv3968
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