A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624866



Internal ID15848402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185520778..185522956hg38UCSC Ensembl
Outerchr4:185519206..185526416hg38UCSC Ensembl
Innerchr4:186441932..186444110hg19UCSC Ensembl
Outerchr4:186440360..186447570hg19UCSC Ensembl
Innerchr4:186678926..186681104hg18UCSC Ensembl
Outerchr4:186677354..186684564hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg387211
hg197211
hg187211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511267
Supporting Variants
Samples1
Known GenesPDLIM3
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624866
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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