A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8973n54



Internal ID22776868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11301584..11328451hg38UCSC Ensembl
chr4:11303208..11330075hg19UCSC Ensembl
chr4:10912306..10939173hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3826868
hg1926868
hg1826868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593737, nsv593735, nsv593734, nsv593736
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8973n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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