A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13385778



Internal ID5641488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6034482..6039827hg38UCSC Ensembl
Innerchr9:6034482..6039827hg38UCSC Ensembl
Outerchr9:6034351..6039978hg38UCSC Ensembl
chr9:6034482..6039827hg19UCSC Ensembl
Innerchr9:6034482..6039827hg19UCSC Ensembl
Outerchr9:6034351..6039978hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385346
hg195346
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619392
Supporting Variants
SamplesNA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13385778
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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