A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585936



Internal ID6973455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46418566..46426663hg38UCSC Ensembl
Innerchr1:46418566..46426663hg38UCSC Ensembl
Outerchr1:46418066..46427163hg38UCSC Ensembl
chr1:46884238..46892335hg19UCSC Ensembl
Innerchr1:46884238..46892335hg19UCSC Ensembl
Outerchr1:46883738..46892835hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg388098
hg198098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9926480
SamplesHG01353
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585936
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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