A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637088



Internal ID7023882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84249185..84402292hg38UCSC Ensembl
chr15:84917937..84956990hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38153108
hg1939054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15313615, essv15313612, essv15313614, essv15313613, essv15313611
SamplesHG03478, HG03397, HG03934, HG03410, HG02465
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637088
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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