A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637198



Internal ID7023992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89527339..89576103hg38UCSC Ensembl
chr15:90070570..90119334hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3848765
hg1948765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317170, essv15317171, essv15317172
SamplesNA12414, NA19461, NA19338
Known GenesTICRR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637198
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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