A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3440



Internal ID15201364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62137705..62169472hg38UCSC Ensembl
Outerchr20:60712761..60744528hg19UCSC Ensembl
Outerchr20:60146156..60177923hg18UCSC Ensembl
Outerchr20:60146156..60177923hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387666
hg197666
hg187666
hg177666
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6947
SamplesNA12156
Known GenesPSMA7, SS18L1
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)nsv3440
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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