A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626810



Internal ID15850343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62875039..62875521hg38UCSC Ensembl
Outerchr20:61506391..61506873hg19UCSC Ensembl
Outerchr20:60976836..60977318hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38972
hg19972
hg18972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513558
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626810
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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