A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636878



Internal ID7023672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72609543..72647982hg38UCSC Ensembl
Innerchr15:72609543..72647982hg38UCSC Ensembl
Outerchr15:72609043..72648482hg38UCSC Ensembl
chr15:72901884..72940323hg19UCSC Ensembl
Innerchr15:72901884..72940323hg19UCSC Ensembl
Outerchr15:72901384..72940823hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3838440
hg1938440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15291503, essv15291504
SamplesHG01932, HG02699
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636878
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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