A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635979



Internal ID7022776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27547705..27549302hg38UCSC Ensembl
Innerchr15:27547739..27549269hg38UCSC Ensembl
Outerchr15:27547672..27549336hg38UCSC Ensembl
chr15:27792851..27794448hg19UCSC Ensembl
Innerchr15:27792885..27794415hg19UCSC Ensembl
Outerchr15:27792818..27794482hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381598
hg191598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15197394, essv15197395
SamplesHG03940, NA20908
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635979
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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