A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13534729



Internal ID857024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79413234..79418530hg38UCSC Ensembl
Innerchr9:79413234..79418530hg38UCSC Ensembl
Outerchr9:79412880..79418866hg38UCSC Ensembl
chr9:82028149..82033445hg19UCSC Ensembl
Innerchr9:82028149..82033445hg19UCSC Ensembl
Outerchr9:82027795..82033781hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385297
hg195297
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620828
Supporting Variants
SamplesHG00448
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13534729
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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