A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256372



Internal ID5258188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55629969..55635099hg38UCSC Ensembl
Innerchr15:55629969..55635099hg38UCSC Ensembl
Outerchr15:55629937..55635158hg38UCSC Ensembl
chr15:55922167..55927297hg19UCSC Ensembl
Innerchr15:55922167..55927297hg19UCSC Ensembl
Outerchr15:55922135..55927356hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385131
hg195131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636567
Supporting Variants
SamplesHG04164
Known GenesPRTG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15256372
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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