A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589916



Internal ID6977246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15583033..15583734hg38UCSC Ensembl
Innerchr2:15583039..15583729hg38UCSC Ensembl
Outerchr2:15583028..15583740hg38UCSC Ensembl
chr2:15723157..15723858hg19UCSC Ensembl
Innerchr2:15723163..15723853hg19UCSC Ensembl
Outerchr2:15723152..15723864hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10417856, essv10417857, essv10417858
SamplesHG01840, HG00867, HG01804
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589916
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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