A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637341



Internal ID7024134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95775313..95786792hg38UCSC Ensembl
Innerchr15:95775463..95786642hg38UCSC Ensembl
Outerchr15:95775163..95786942hg38UCSC Ensembl
chr15:96318542..96330021hg19UCSC Ensembl
Innerchr15:96318692..96329871hg19UCSC Ensembl
Outerchr15:96318392..96330171hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3811480
hg1911480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15327842, essv15327843
SamplesHG00181, NA20911
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637341
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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