A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647763



Internal ID7034502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39361342..39363242hg38UCSC Ensembl
Innerchr22:39361372..39363212hg38UCSC Ensembl
Outerchr22:39361312..39363272hg38UCSC Ensembl
chr22:39757347..39759247hg19UCSC Ensembl
Innerchr22:39757377..39759217hg19UCSC Ensembl
Outerchr22:39757317..39759277hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16427801
SamplesHG03557
Known GenesSYNGR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647763
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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