A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637523



Internal ID7024315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101687508..101689562hg38UCSC Ensembl
Innerchr15:101687513..101689557hg38UCSC Ensembl
Outerchr15:101687503..101689567hg38UCSC Ensembl
chr15:102227711..102229765hg19UCSC Ensembl
Innerchr15:102227716..102229760hg19UCSC Ensembl
Outerchr15:102227706..102229770hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15354530, essv15354529
SamplesNA18520, NA19118
Known GenesTARSL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637523
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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