A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5644n100



Internal ID22791731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:46101743..46389159hg38UCSC Ensembl
chr5:46101845..46389261hg19UCSC Ensembl
chr5:46137602..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38287417
hg19287417
hg18287417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028712, nsv1018733, nsv1028954, nsv1019374, nsv1029174, nsv1034670, nsv1027538
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)dgv5644n100
Frequency
Sample Size11257
Observed Gain33
Observed Loss0
Observed Complex0
Frequencyn/a


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