A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5052n100



Internal ID22791139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12269..51612hg38UCSC Ensembl
chr4:12269..51506hg19UCSC Ensembl
chr4:2269..41506hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839344
hg1939238
hg1839238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012666, nsv1008424, nsv1014360, nsv1010913
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5052n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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