A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647897



Internal ID7034636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44355395..44367787hg38UCSC Ensembl
Innerchr22:44355395..44367787hg38UCSC Ensembl
Outerchr22:44354895..44368287hg38UCSC Ensembl
chr22:44751275..44763667hg19UCSC Ensembl
Innerchr22:44751275..44763667hg19UCSC Ensembl
Outerchr22:44750775..44764167hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3812393
hg1912393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16437481
SamplesHG04060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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