A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600112



Internal ID6987156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32325867..32348377hg38UCSC Ensembl
chr4:32327489..32349999hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3822511
hg1922511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11388095, essv11388094
SamplesHG01761, NA20334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600112
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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