A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637366



Internal ID7024159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97108203..97109332hg38UCSC Ensembl
Innerchr15:97108209..97109327hg38UCSC Ensembl
Outerchr15:97108198..97109338hg38UCSC Ensembl
chr15:97651433..97652562hg19UCSC Ensembl
Innerchr15:97651439..97652557hg19UCSC Ensembl
Outerchr15:97651428..97652568hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381130
hg191130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15331124, essv15331125, essv15331123
SamplesHG02691, HG02690, HG02655
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637366
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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