A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15283139



Internal ID2624356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70456207..70457036hg38UCSC Ensembl
Innerchr15:70456207..70457036hg38UCSC Ensembl
Outerchr15:70456023..70457366hg38UCSC Ensembl
chr15:70748546..70749375hg19UCSC Ensembl
Innerchr15:70748546..70749375hg19UCSC Ensembl
Outerchr15:70748362..70749705hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636837
Supporting Variants
SamplesHG02322
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15283139
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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