A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6461793



Internal ID9439196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17877139..17877412hg38UCSC Ensembl
Outerchr22:17877102..17877462hg38UCSC Ensembl
Innerchr22:18359905..18360178hg19UCSC Ensembl
Outerchr22:18359868..18360228hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670806
Supporting Variants
SamplesNA20348
Known GenesMICAL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6461793
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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