A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637279



Internal ID7024073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93126601..93129360hg38UCSC Ensembl
Innerchr15:93126602..93129360hg38UCSC Ensembl
Outerchr15:93126601..93129361hg38UCSC Ensembl
chr15:93669830..93672589hg19UCSC Ensembl
Innerchr15:93669831..93672589hg19UCSC Ensembl
Outerchr15:93669830..93672590hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382760
hg192760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15321831
SamplesHG02107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637279
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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