A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5755n100



Internal ID22791842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:104361328..104453791hg38UCSC Ensembl
chr5:103697029..103789492hg19UCSC Ensembl
chr5:103724928..103817391hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3892464
hg1992464
hg1892464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021195, nsv1034834, nsv1030008, nsv1021408
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)dgv5755n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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