A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511624



Internal ID15851049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1409129..1410038hg38UCSC Ensembl
Outerchr20:1407932..1410792hg38UCSC Ensembl
Innerchr20:1389773..1390682hg19UCSC Ensembl
Outerchr20:1388576..1391436hg19UCSC Ensembl
Innerchr20:1337773..1338682hg18UCSC Ensembl
Outerchr20:1336576..1339436hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382861
hg192861
hg182861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626257
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511624
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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