A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16410938



Internal ID3568807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34710482..34721260hg38UCSC Ensembl
Innerchr22:34710501..34721242hg38UCSC Ensembl
Outerchr22:34710464..34721279hg38UCSC Ensembl
chr22:35106473..35117251hg19UCSC Ensembl
Innerchr22:35106492..35117233hg19UCSC Ensembl
Outerchr22:35106455..35117270hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3810779
hg1910779
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647649
Supporting Variants
SamplesHG03159
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16410938
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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