A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647899



Internal ID7034638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44423774..44425269hg38UCSC Ensembl
Innerchr22:44423774..44425269hg38UCSC Ensembl
Outerchr22:44423589..44425269hg38UCSC Ensembl
chr22:44819654..44821149hg19UCSC Ensembl
Innerchr22:44819654..44821149hg19UCSC Ensembl
Outerchr22:44819469..44821149hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16437483
SamplesHG00653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647899
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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