A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15289601



Internal ID3720128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72279581..72283242hg38UCSC Ensembl
Innerchr15:72279582..72283242hg38UCSC Ensembl
Outerchr15:72279581..72283243hg38UCSC Ensembl
chr15:72571922..72575583hg19UCSC Ensembl
Innerchr15:72571923..72575583hg19UCSC Ensembl
Outerchr15:72571922..72575584hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383662
hg193662
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636872
Supporting Variants
SamplesHG03351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15289601
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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