A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3436



Internal ID15548045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:61118237..61127596hg38UCSC Ensembl
Outerchr20:59693293..59702652hg19UCSC Ensembl
Outerchr20:59126688..59136047hg18UCSC Ensembl
Outerchr20:59126688..59136047hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386077
hg196077
hg186077
hg176077
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7700
SamplesNA12156
Known Genes
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)nsv3436
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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