A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6488432



Internal ID9628138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36455643..36456865hg38UCSC Ensembl
chr22:36851690..36852912hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673935
Supporting Variants
SamplesNA19350
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6488432
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