A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3959



Internal ID15548620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:118766205..118811034hg38UCSC Ensembl
Outerchr3:118485052..118529881hg19UCSC Ensembl
Outerchr3:119967742..120012571hg18UCSC Ensembl
Outerchr3:119967742..120012571hg17UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3844830
hg1944830
hg1844830
hg1744830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7849
SamplesNA12156
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)nsv3959
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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