A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644979



Internal ID7031730
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16111533, essv16111534
SamplesHG02722, HG03039
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644979
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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