A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271850



Internal ID3697040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65326066..65326464hg38UCSC Ensembl
Innerchr15:65326067..65326463hg38UCSC Ensembl
Outerchr15:65326065..65326465hg38UCSC Ensembl
chr15:65618404..65618802hg19UCSC Ensembl
Innerchr15:65618405..65618801hg19UCSC Ensembl
Outerchr15:65618403..65618803hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636754
Supporting Variants
SamplesHG03300
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271850
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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