A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16163895



Internal ID6165711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23821040..23860450hg38UCSC Ensembl
chr20:23801677..23841087hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3839411
hg1939411
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645537
Supporting Variants
SamplesNA18644
Known GenesCST2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16163895
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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