A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625957



Internal ID15849490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25066367..25067148hg38UCSC Ensembl
Outerchr20:25047003..25047784hg19UCSC Ensembl
Outerchr20:24995003..24995784hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513541
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)nssv625957
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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