A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10415053



Internal ID2005748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15003909..15076710hg38UCSC Ensembl
chr2:15144033..15216834hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3872802
hg1972802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3589902
Supporting Variants
SamplesHG01853
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10415053
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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