A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15233736



Internal ID2214806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45227371..45229137hg38UCSC Ensembl
Innerchr15:45227372..45229137hg38UCSC Ensembl
Outerchr15:45227371..45229138hg38UCSC Ensembl
chr15:45519569..45521335hg19UCSC Ensembl
Innerchr15:45519570..45521335hg19UCSC Ensembl
Outerchr15:45519569..45521336hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381767
hg191767
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636334
Supporting Variants
SamplesHG01990
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15233736
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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