A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5635n100



Internal ID22791722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38741127..38791546hg38UCSC Ensembl
chr5:38741229..38791648hg19UCSC Ensembl
chr5:38776986..38827405hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3850420
hg1950420
hg1850420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017826, nsv1033254
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)dgv5635n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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