A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15266020



Internal ID5267836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62255972..62260221hg38UCSC Ensembl
Innerchr15:62256022..62260171hg38UCSC Ensembl
Outerchr15:62255858..62260335hg38UCSC Ensembl
chr15:62548171..62552420hg19UCSC Ensembl
Innerchr15:62548221..62552370hg19UCSC Ensembl
Outerchr15:62548057..62552534hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384250
hg194250
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636695
Supporting Variants
SamplesHG03887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15266020
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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