A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636939



Internal ID7023733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76381983..76384755hg38UCSC Ensembl
Innerchr15:76382042..76384697hg38UCSC Ensembl
Outerchr15:76381925..76384814hg38UCSC Ensembl
chr15:76674324..76677096hg19UCSC Ensembl
Innerchr15:76674383..76677038hg19UCSC Ensembl
Outerchr15:76674266..76677155hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382773
hg192773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15295762, essv15295763
SamplesHG00534, NA18747
Known GenesSCAPER
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636939
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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