A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646859



Internal ID7033602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31373838..31390964hg38UCSC Ensembl
chr21:32746152..32763277hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3817127
hg1917126
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv811e214
Supporting Variantsessv16311927
SamplesHG00157
Known GenesTIAM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646859
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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