A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589370



Internal ID6976698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:242580447..242621304hg38UCSC Ensembl
chr1:242743749..242784606hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3840858
hg1940858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10356777, essv10356778, essv10356779
SamplesHG02266, HG02395, HG01565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589370
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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