A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637476



Internal ID7024268
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15352138, essv15352137
SamplesHG03844, HG03714
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637476
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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