A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635910



Internal ID6676020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24864194..24872030hg38UCSC Ensembl
Innerchr15:24864194..24872030hg38UCSC Ensembl
Outerchr15:24863694..24872530hg38UCSC Ensembl
chr15:25109341..25117177hg19UCSC Ensembl
Innerchr15:25109341..25117177hg19UCSC Ensembl
Outerchr15:25108841..25117677hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387837
hg197837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15185096, essv15185097, essv15185095, essv15185094
SamplesNA19083, NA19000, NA19005, NA18962
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635910
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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