A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660656



Internal ID9926761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21417027..21434833hg38UCSC Ensembl
Outerchr22:21416656..21435203hg38UCSC Ensembl
Innerchr22:21771316..21789122hg19UCSC Ensembl
Outerchr22:21770945..21789492hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3818548
hg1918548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5554645, essv5994416, essv6499155, essv5666709, essv6070464, essv5608229, essv5534618, essv6009794, essv6509295, essv6107256, essv5750597, essv5780866, essv5699084, essv5975959, essv5550290, essv5476251, essv5777541, essv5957015, essv5448691
SamplesHG01441, HG01462, HG01389, HG01374, HG01461, HG01140, HG01366, HG01351, HG01365, HG01134, HG01440, HG01353, HG01360, HG01149, HG01148, HG01375, HG01113, HG01377, HG01125
Known GenesHIC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660656
Frequency
Sample Size1151
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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