A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6088124



Internal ID8724592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34007779..34010974hg38UCSC Ensembl
Outerchr22:34007622..34011127hg38UCSC Ensembl
Innerchr22:34403768..34406963hg19UCSC Ensembl
Outerchr22:34403611..34407116hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383506
hg193506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667115
Supporting Variants
SamplesHG00108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6088124
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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