A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6310801



Internal ID9288204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27790628..27804034hg38UCSC Ensembl
Outerchr22:27790257..27804404hg38UCSC Ensembl
Innerchr22:28186616..28200022hg19UCSC Ensembl
Outerchr22:28186245..28200392hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3814148
hg1914148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675305
Supporting Variants
SamplesNA19346
Known GenesMN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6310801
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer