A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635991



Internal ID6676101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28132541..28198997hg38UCSC Ensembl
chr15:28377687..28444143hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3866457
hg1966457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15198899, essv15198900, essv15198898
SamplesNA18489, HG02143, HG03039
Known GenesHERC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635991
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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