A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637132



Internal ID6677239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86085527..86089576hg38UCSC Ensembl
Innerchr15:86085527..86089576hg38UCSC Ensembl
Outerchr15:86085260..86089836hg38UCSC Ensembl
chr15:86628758..86632807hg19UCSC Ensembl
Innerchr15:86628758..86632807hg19UCSC Ensembl
Outerchr15:86628491..86633067hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv458e214
Supporting Variantsessv15315902, essv15315901
SamplesHG00445, NA18552
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637132
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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