A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3719



Internal ID15201670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:20091751..20108710hg38UCSC Ensembl
Outerchr3:20133243..20150202hg19UCSC Ensembl
Outerchr3:20108247..20125206hg18UCSC Ensembl
Outerchr3:20108247..20125206hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3816960
hg1916960
hg1816960
hg1716960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7774
SamplesNA12156
Known GenesKAT2B
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)nsv3719
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