A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3963



Internal ID15201939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:119582217..119627057hg38UCSC Ensembl
Outerchr3:119301064..119345904hg19UCSC Ensembl
Outerchr3:120783754..120828594hg18UCSC Ensembl
Outerchr3:120783754..120828594hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3844841
hg1944841
hg1844841
hg1744841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7851
SamplesNA12156
Known GenesADPRH, PLA1A
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)nsv3963
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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