A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16411336



Internal ID6413152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35064756..35171556hg38UCSC Ensembl
Innerchr22:35064802..35171511hg38UCSC Ensembl
Outerchr22:35064711..35171602hg38UCSC Ensembl
chr22:35460749..35567549hg19UCSC Ensembl
Innerchr22:35460795..35567504hg19UCSC Ensembl
Outerchr22:35460704..35567595hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38106801
hg19106801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647659
Supporting Variants
SamplesNA18612
Known GenesISX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16411336
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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