A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637522



Internal ID6677626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101670226..101754487hg38UCSC Ensembl
chr15:102210429..102294690hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3884262
hg1984262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15354528, essv15354527, essv15354526
SamplesHG01762, NA12827, HG02813
Known GenesTARSL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637522
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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