A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5877



Internal ID15543510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:40306926..40339843hg38UCSC Ensembl
Outerchr20:38935566..38968483hg19UCSC Ensembl
Outerchr20:38368980..38401897hg18UCSC Ensembl
Outerchr20:38368980..38401897hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg386300
hg196300
hg186300
hg176300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3377
Supporting Variants
SamplesNA19129
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)nssv5877
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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