A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13532967



Internal ID1925178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78547481..78553545hg38UCSC Ensembl
chr9:81162397..81168461hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg386065
hg196065
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620799
Supporting Variants
SamplesHG01798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13532967
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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