A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15198898



Internal ID5200714
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635991
Supporting Variants
SamplesHG02143
Known GenesHERC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15198898
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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