A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13571990



Internal ID511748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95712640..95717072hg38UCSC Ensembl
Innerchr9:95712640..95717072hg38UCSC Ensembl
Outerchr9:95712524..95717217hg38UCSC Ensembl
chr9:98474922..98479354hg19UCSC Ensembl
Innerchr9:98474922..98479354hg19UCSC Ensembl
Outerchr9:98474806..98479499hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384433
hg194433
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621156
Supporting Variants
SamplesHG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13571990
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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