A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16179809



Internal ID6181625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36533223..36534274hg38UCSC Ensembl
Innerchr20:36533223..36534274hg38UCSC Ensembl
Outerchr20:36532955..36534496hg38UCSC Ensembl
chr20:35161626..35162677hg19UCSC Ensembl
Innerchr20:35161626..35162677hg19UCSC Ensembl
Outerchr20:35161358..35162899hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645737
Supporting Variants
SamplesNA19462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16179809
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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