A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5791n100



Internal ID22791878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116190652..116279762hg38UCSC Ensembl
chr5:115526349..115615459hg19UCSC Ensembl
chr5:115554248..115643358hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3889111
hg1989111
hg1889111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032799, nsv1024670, nsv1016924, nsv1016585, nsv1019540
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5791n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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