A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636282



Internal ID7023078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42837193..42838064hg38UCSC Ensembl
Innerchr15:42837243..42838014hg38UCSC Ensembl
Outerchr15:42837143..42838114hg38UCSC Ensembl
chr15:43129391..43130262hg19UCSC Ensembl
Innerchr15:43129441..43130212hg19UCSC Ensembl
Outerchr15:43129341..43130312hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231118
SamplesHG02522
Known GenesTTBK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636282
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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