A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511243



Internal ID15850668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6650434..6651073hg38UCSC Ensembl
Outerchr4:6648839..6661592hg38UCSC Ensembl
Innerchr4:6652161..6652800hg19UCSC Ensembl
Outerchr4:6650566..6663319hg19UCSC Ensembl
Innerchr4:6703062..6703701hg18UCSC Ensembl
Outerchr4:6701467..6714220hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3812754
hg1912754
hg1812754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624600
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)nsv511243
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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