A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511538



Internal ID15850963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101711842..101713702hg38UCSC Ensembl
Outerchr14:101691436..101717022hg38UCSC Ensembl
Innerchr14:102178179..102180039hg19UCSC Ensembl
Outerchr14:102157773..102183359hg19UCSC Ensembl
Innerchr14:101247932..101249792hg18UCSC Ensembl
Outerchr14:101227526..101253112hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3825587
hg1925587
hg1825587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626161
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)nsv511538
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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