A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637204



Internal ID6677311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89853490..89866540hg38UCSC Ensembl
chr15:90396722..90409772hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3813051
hg1913051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317184, essv15317182, essv15317183, essv15317181, essv15317180
SamplesHG03091, NA20757, HG02715, HG03547, NA19000
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637204
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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