A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645833



Internal ID6685894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41097670..41103447hg38UCSC Ensembl
Innerchr20:41097670..41103447hg38UCSC Ensembl
Outerchr20:41097170..41103947hg38UCSC Ensembl
chr20:39726310..39732087hg19UCSC Ensembl
Innerchr20:39726310..39732087hg19UCSC Ensembl
Outerchr20:39725810..39732587hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg385778
hg195778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16186695
SamplesNA12004
Known GenesTOP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645833
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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