A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933



Internal ID15201906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:107098118..107143050hg38UCSC Ensembl
Outerchr3:106816965..106861897hg19UCSC Ensembl
Outerchr3:108299655..108344587hg18UCSC Ensembl
Outerchr3:108299655..108344587hg17UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3844933
hg1944933
hg1844933
hg1744933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7841
SamplesNA12156
Known GenesLINC00882
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)nsv3933
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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