A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589847



Internal ID6977177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13494909..13549721hg38UCSC Ensembl
chr2:13635034..13689846hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3854813
hg1954813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv676e214
Supporting Variantsessv10412838, essv10412839
SamplesNA18988, HG04141
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589847
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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