A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511620



Internal ID15851045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36267237..36310296hg38UCSC Ensembl
Outerchr19:36258902..36311000hg38UCSC Ensembl
Innerchr19:36758139..36801198hg19UCSC Ensembl
Outerchr19:36749804..36801902hg19UCSC Ensembl
Innerchr19:41449979..41493038hg18UCSC Ensembl
Outerchr19:41441644..41493742hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852099
hg1952099
hg1852099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626251
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)nsv511620
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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