A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647262



Internal ID7034003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19156774..19169573hg38UCSC Ensembl
Innerchr22:19157274..19169073hg38UCSC Ensembl
Outerchr22:19155774..19170573hg38UCSC Ensembl
chr22:19144287..19157086hg19UCSC Ensembl
Innerchr22:19144787..19156586hg19UCSC Ensembl
Outerchr22:19143287..19158086hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16364963, essv16364962, essv16364964
SamplesNA18641, NA19917, HG03488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647262
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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