A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16111534



Internal ID3388603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1424723..1425957hg38UCSC Ensembl
Innerchr20:1424732..1425948hg38UCSC Ensembl
Outerchr20:1424714..1425966hg38UCSC Ensembl
chr20:1405367..1406601hg19UCSC Ensembl
Innerchr20:1405376..1406592hg19UCSC Ensembl
Outerchr20:1405358..1406610hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644979
Supporting Variants
SamplesHG03039
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16111534
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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