A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635980



Internal ID7022777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27647583..27658669hg38UCSC Ensembl
Innerchr15:27647592..27658661hg38UCSC Ensembl
Outerchr15:27647575..27658678hg38UCSC Ensembl
chr15:27892729..27903815hg19UCSC Ensembl
Innerchr15:27892738..27903807hg19UCSC Ensembl
Outerchr15:27892721..27903824hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3811087
hg1911087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15197396
SamplesHG00141
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635980
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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