A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3367



Internal ID15547969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:35859973..35893307hg38UCSC Ensembl
Outerchr20:34447895..34481229hg19UCSC Ensembl
Outerchr20:33911309..33944643hg18UCSC Ensembl
Outerchr20:33911309..33944643hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg386106
hg196106
hg186106
hg176106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7677
SamplesNA12156
Known GenesPHF20
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)nsv3367
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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