A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15306761



Internal ID4837612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81481333..81489239hg38UCSC Ensembl
Innerchr15:81481372..81489200hg38UCSC Ensembl
Outerchr15:81481294..81489278hg38UCSC Ensembl
chr15:81773674..81781580hg19UCSC Ensembl
Innerchr15:81773713..81781541hg19UCSC Ensembl
Outerchr15:81773635..81781619hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387907
hg197907
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637036
Supporting Variants
SamplesNA12154
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15306761
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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