A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15352137



Internal ID4086924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100378829..100383128hg38UCSC Ensembl
Innerchr15:100378855..100383103hg38UCSC Ensembl
Outerchr15:100378804..100383154hg38UCSC Ensembl
chr15:100919034..100923333hg19UCSC Ensembl
Innerchr15:100919060..100923308hg19UCSC Ensembl
Outerchr15:100919009..100923359hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637476
Supporting Variants
SamplesHG03714
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15352137
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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