A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13615565



Internal ID4240660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121642907..121643817hg38UCSC Ensembl
Innerchr9:121642907..121643817hg38UCSC Ensembl
Outerchr9:121642566..121644141hg38UCSC Ensembl
chr9:124405186..124406096hg19UCSC Ensembl
Innerchr9:124405186..124406096hg19UCSC Ensembl
Outerchr9:124404845..124406420hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621667
Supporting Variants
SamplesHG03814
Known GenesDAB2IP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13615565
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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