A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15312471



Internal ID5314287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83486014..83536809hg38UCSC Ensembl
Innerchr15:83486014..83536809hg38UCSC Ensembl
Outerchr15:83485514..83537309hg38UCSC Ensembl
chr15:84154766..84205561hg19UCSC Ensembl
Innerchr15:84154766..84205561hg19UCSC Ensembl
Outerchr15:84154266..84206061hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3850796
hg1950796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637073
Supporting Variants
SamplesHG02307
Known GenesSH3GL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15312471
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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