A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv776e199



Internal ID20124078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3898151..3904682hg38UCSC Ensembl
chr20:3878798..3885329hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386532
hg196532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672145, esv2656799
SamplesHG01188, NA19684, NA19720, HG00268, NA19783, HG00312, NA19726
Known GenesPANK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv776e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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