A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8943n54



Internal ID22776838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7254893..7309672hg38UCSC Ensembl
chr4:7256620..7311399hg19UCSC Ensembl
chr4:7307521..7362300hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3854780
hg1954780
hg1854780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593568, nsv593567
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8943n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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