A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626152



Internal ID15849685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:60591339..60592635hg38UCSC Ensembl
Outerchr14:60556071..60594581hg38UCSC Ensembl
Innerchr14:61058057..61059353hg19UCSC Ensembl
Outerchr14:61022789..61061299hg19UCSC Ensembl
Innerchr14:60127810..60129106hg18UCSC Ensembl
Outerchr14:60092542..60131052hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3838511
hg1938511
hg1838511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511530
Supporting Variants
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)nssv626152
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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