A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637019



Internal ID7023813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80504412..80507675hg38UCSC Ensembl
Innerchr15:80504426..80507662hg38UCSC Ensembl
Outerchr15:80504399..80507689hg38UCSC Ensembl
chr15:80796753..80800016hg19UCSC Ensembl
Innerchr15:80796767..80800003hg19UCSC Ensembl
Outerchr15:80796740..80800030hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383264
hg193264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15305447, essv15305446
SamplesHG04131, HG04029
Known GenesARNT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637019
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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