A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646310



Internal ID7033055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63370107..63376267hg38UCSC Ensembl
Innerchr20:63370607..63375767hg38UCSC Ensembl
Outerchr20:63369107..63377267hg38UCSC Ensembl
chr20:62001459..62007619hg19UCSC Ensembl
Innerchr20:62001959..62007119hg19UCSC Ensembl
Outerchr20:62000459..62008619hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386161
hg196161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16229466, essv16229467, essv16229465
SamplesHG02786, HG03709, NA21143
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646310
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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