A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637208



Internal ID7024002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89962207..89967672hg38UCSC Ensembl
Innerchr15:89962257..89967622hg38UCSC Ensembl
Outerchr15:89962157..89967722hg38UCSC Ensembl
chr15:90505439..90510904hg19UCSC Ensembl
Innerchr15:90505489..90510854hg19UCSC Ensembl
Outerchr15:90505389..90510954hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385466
hg195466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317200, essv15317206, essv15317208, essv15317209, essv15317212, essv15317201, essv15317210, essv15317199, essv15317211, essv15317205, essv15317207, essv15317202, essv15317204, essv15317203
SamplesHG03130, NA19092, NA20332, HG03499, HG01170, NA19917, NA20412, HG02623, NA19152, HG03136, NA18523, NA18909, HG03304, NA20348
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637208
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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