A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647636



Internal ID7034376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33998782..34103087hg38UCSC Ensembl
Innerchr22:33998924..34102945hg38UCSC Ensembl
Outerchr22:33998640..34103229hg38UCSC Ensembl
chr22:34394771..34499076hg19UCSC Ensembl
Innerchr22:34394913..34498934hg19UCSC Ensembl
Outerchr22:34394629..34499218hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38104306
hg19104306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16408907, essv16408904, essv16408905, essv16408903, essv16408906
SamplesNA19466, NA19315, NA19391, NA19043, NA19468
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647636
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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