A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5819n100



Internal ID22791906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152131484..152144649hg38UCSC Ensembl
chr5:151511045..151524210hg19UCSC Ensembl
chr5:151491238..151504403hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3813166
hg1913166
hg1813166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016168, nsv1028974, nsv1032207
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)dgv5819n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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