A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv135e199



Internal ID20123437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46372885..46397776hg38UCSC Ensembl
chr10:47744145..47769042hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3824892
hg1924898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664704, esv2661207
SamplesNA19712, NA19904, NA20278, NA19783, NA20346, NA20294, NA19788, NA20342, NA19782, NA19651, NA19678, NA20322, NA19914, NA19917, NA19675, NA20127, NA19908, NA19985, NA19835, NA20282, NA19679, NA19684, NA19728, NA19676, NA19725, NA19786, NA20291, NA19703, NA20126, NA20348, NA19716, NA19664, NA19901, NA19704, NA19909, NA19720, NA19711, NA19777, NA19921, NA19723, NA20289, NA19719, NA20287, NA19717, NA19916, NA19750
Known GenesANXA8L1, ANXA8L2, FAM25B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv135e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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