A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16186856



Internal ID6188672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41277705..41278888hg38UCSC Ensembl
Innerchr20:41277705..41278888hg38UCSC Ensembl
Outerchr20:41277705..41278888hg38UCSC Ensembl
chr20:39906345..39907528hg19UCSC Ensembl
Innerchr20:39906345..39907528hg19UCSC Ensembl
Outerchr20:39906345..39907528hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645835
Supporting Variants
SamplesHG01308
Known GenesZHX3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16186856
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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