A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586367



Internal ID6626680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70885560..70901337hg38UCSC Ensembl
chr1:71351243..71367020hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3815778
hg1915778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv22e214
Supporting Variantsessv9964783, essv9964784, essv9964781, essv9964782
SamplesHG00177, HG00182, NA21124, NA20908
Known GenesPTGER3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586367
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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