A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636883



Internal ID7023677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73000300..73014269hg38UCSC Ensembl
Innerchr15:73000316..73014253hg38UCSC Ensembl
Outerchr15:73000284..73014285hg38UCSC Ensembl
chr15:73292641..73306610hg19UCSC Ensembl
Innerchr15:73292657..73306594hg19UCSC Ensembl
Outerchr15:73292625..73306626hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3813970
hg1913970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15291519
SamplesHG01619
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636883
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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