A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16382535



Internal ID6384351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23234660..23235620hg38UCSC Ensembl
Innerchr22:23234660..23235620hg38UCSC Ensembl
Outerchr22:23234660..23235620hg38UCSC Ensembl
chr22:23576847..23577807hg19UCSC Ensembl
Innerchr22:23576847..23577807hg19UCSC Ensembl
Outerchr22:23576847..23577807hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647396
Supporting Variants
SamplesHG01414
Known GenesBCR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16382535
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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