A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5670n100



Internal ID22791757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56355995..56368070hg38UCSC Ensembl
chr5:55651822..55663897hg19UCSC Ensembl
chr5:55687579..55699654hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3812076
hg1912076
hg1812076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026668, nsv1019866, nsv1025241
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)dgv5670n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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