A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636647



Internal ID6676754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59650139..59669840hg38UCSC Ensembl
chr15:59942338..59962039hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3819702
hg1919702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261109
SamplesHG04210
Known GenesBNIP2, GTF2A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636647
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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