A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585868



Internal ID6973388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43454812..43456560hg38UCSC Ensembl
Innerchr1:43454830..43456543hg38UCSC Ensembl
Outerchr1:43454795..43456578hg38UCSC Ensembl
chr1:43920483..43922231hg19UCSC Ensembl
Innerchr1:43920501..43922214hg19UCSC Ensembl
Outerchr1:43920466..43922249hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381749
hg191749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9921755
SamplesHG03814
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585868
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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