A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15249460



Internal ID3501539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53048159..53076656hg38UCSC Ensembl
Innerchr15:53048170..53076646hg38UCSC Ensembl
Outerchr15:53048149..53076667hg38UCSC Ensembl
chr15:53340356..53368853hg19UCSC Ensembl
Innerchr15:53340367..53368843hg19UCSC Ensembl
Outerchr15:53340346..53368864hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3828498
hg1928498
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636501
Supporting Variants
SamplesHG03108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15249460
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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