A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646180



Internal ID7032925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56052089..56091422hg38UCSC Ensembl
Innerchr20:56052089..56091422hg38UCSC Ensembl
Outerchr20:56051589..56091922hg38UCSC Ensembl
chr20:54627145..54666478hg19UCSC Ensembl
Innerchr20:54627145..54666478hg19UCSC Ensembl
Outerchr20:54626645..54666978hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3839334
hg1939334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16213336
SamplesHG03708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646180
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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