A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511628



Internal ID15851053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7419155..7422657hg38UCSC Ensembl
Outerchr20:7408420..7423699hg38UCSC Ensembl
Innerchr20:7399802..7403304hg19UCSC Ensembl
Outerchr20:7389067..7404346hg19UCSC Ensembl
Innerchr20:7347802..7351304hg18UCSC Ensembl
Outerchr20:7337067..7352346hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3815280
hg1915280
hg1815280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626261
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)nsv511628
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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