A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647503



Internal ID7034244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28169595..28197429hg38UCSC Ensembl
Innerchr22:28170095..28196929hg38UCSC Ensembl
Outerchr22:28168595..28198429hg38UCSC Ensembl
chr22:28565583..28593417hg19UCSC Ensembl
Innerchr22:28566083..28592917hg19UCSC Ensembl
Outerchr22:28564583..28594417hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3827835
hg1927835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv836e214
Supporting Variantsessv16397312
SamplesHG03742
Known GenesTTC28
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647503
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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