A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5669n100



Internal ID22791756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54646174..54686985hg38UCSC Ensembl
chr5:53942003..53982814hg19UCSC Ensembl
chr5:53977760..54018571hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3840812
hg1940812
hg1840812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026231, nsv1027583
Samples
Known GenesLOC102467080
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5669n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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