A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15221232



Internal ID2420296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38829249..38838738hg38UCSC Ensembl
Innerchr15:38829249..38838738hg38UCSC Ensembl
Outerchr15:38828749..38839238hg38UCSC Ensembl
chr15:39121450..39130939hg19UCSC Ensembl
Innerchr15:39121450..39130939hg19UCSC Ensembl
Outerchr15:39120950..39131439hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389490
hg199490
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636202
Supporting Variants
SamplesHG02140
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15221232
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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