A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637519



Internal ID6677623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101606509..101661404hg38UCSC Ensembl
chr15:102146712..102201607hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3854896
hg1954896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15354521, essv15354522
SamplesHG01762, HG02813
Known GenesTARSL2, TM2D3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637519
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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