A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15313665



Internal ID6404134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84699744..84700547hg38UCSC Ensembl
Innerchr15:84699769..84700522hg38UCSC Ensembl
Outerchr15:84699719..84700572hg38UCSC Ensembl
chr15:85242975..85243778hg19UCSC Ensembl
Innerchr15:85243000..85243753hg19UCSC Ensembl
Outerchr15:85242950..85243803hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637098
Supporting Variants
SamplesNA20351
Known GenesSEC11A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15313665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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