A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5672n100



Internal ID22791759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57358610..57442535hg38UCSC Ensembl
chr5:56654437..56738362hg19UCSC Ensembl
chr5:56690194..56774119hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3883926
hg1983926
hg1883926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033378, nsv1026845, nsv1028216
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)dgv5672n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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