A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3264



Internal ID15201170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:3473559..3506248hg38UCSC Ensembl
Outerchr20:3454206..3486895hg19UCSC Ensembl
Outerchr20:3402206..3434895hg18UCSC Ensembl
Outerchr20:3402206..3434895hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386562
hg196562
hg186562
hg176562
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5864
SamplesNA19129
Known GenesATRN
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)nsv3264
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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