A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13431966



Internal ID1257382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24208070..24266179hg38UCSC Ensembl
Innerchr9:24208070..24266179hg38UCSC Ensembl
Outerchr9:24207570..24266679hg38UCSC Ensembl
chr9:24208068..24266177hg19UCSC Ensembl
Innerchr9:24208068..24266177hg19UCSC Ensembl
Outerchr9:24207568..24266677hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3858110
hg1958110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620029
Supporting Variants
SamplesHG01108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13431966
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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