A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644960



Internal ID7031711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:719652..720807hg38UCSC Ensembl
Innerchr20:719673..720787hg38UCSC Ensembl
Outerchr20:719632..720828hg38UCSC Ensembl
chr20:700296..701451hg19UCSC Ensembl
Innerchr20:700317..701431hg19UCSC Ensembl
Outerchr20:700276..701472hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16108957, essv16108963, essv16108965, essv16108959, essv16108962, essv16108958, essv16108960, essv16108964, essv16108966, essv16108961
SamplesHG03479, NA19209, HG02943, NA19099, HG02586, HG03419, HG03039, NA19248, HG03097, HG03538
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644960
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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