A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3413



Internal ID15201334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:50017926..50048795hg38UCSC Ensembl
Outerchr20:48634463..48665332hg19UCSC Ensembl
Outerchr20:48067870..48098739hg18UCSC Ensembl
Outerchr20:48067870..48098739hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg388640
hg198640
hg188640
hg178640
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10300
SamplesNA18956
Known GenesTRERNA1
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)nsv3413
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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