A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637295



Internal ID7024089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93501965..93506934hg38UCSC Ensembl
Innerchr15:93501971..93506928hg38UCSC Ensembl
Outerchr15:93501959..93506940hg38UCSC Ensembl
chr15:94045194..94050163hg19UCSC Ensembl
Innerchr15:94045200..94050157hg19UCSC Ensembl
Outerchr15:94045188..94050169hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384970
hg194970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15321906
SamplesHG02562
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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