A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15313667



Internal ID5728251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84883478..84885266hg38UCSC Ensembl
Innerchr15:84883478..84885266hg38UCSC Ensembl
Outerchr15:84883231..84885453hg38UCSC Ensembl
chr15:85426709..85428497hg19UCSC Ensembl
Innerchr15:85426709..85428497hg19UCSC Ensembl
Outerchr15:85426462..85428684hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381789
hg191789
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637100
Supporting Variants
SamplesNA19107
Known GenesSLC28A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15313667
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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