A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586175



Internal ID6973695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59104446..59109185hg38UCSC Ensembl
Innerchr1:59104458..59109173hg38UCSC Ensembl
Outerchr1:59104434..59109197hg38UCSC Ensembl
chr1:59570118..59574857hg19UCSC Ensembl
Innerchr1:59570130..59574845hg19UCSC Ensembl
Outerchr1:59570106..59574869hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg384740
hg194740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9942316
SamplesHG03111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586175
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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