A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13118986



Internal ID3120802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16087881..16166383hg38UCSC Ensembl
Innerchr8:16087899..16166365hg38UCSC Ensembl
Outerchr8:16087863..16166401hg38UCSC Ensembl
chr8:15945390..16023892hg19UCSC Ensembl
Innerchr8:15945408..16023874hg19UCSC Ensembl
Outerchr8:15945372..16023910hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3878503
hg1978503
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616430
Supporting Variants
SamplesHG03746
Known GenesMSR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13118986
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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