A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636136



Internal ID7022932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35409903..35430253hg38UCSC Ensembl
chr15:35702104..35722454hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3820351
hg1920351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15214190, essv15214191, essv15214189
SamplesNA19067, NA18988, HG00262
Known GenesDPH6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636136
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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