A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13594645



Internal ID4198252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107917689..107920649hg38UCSC Ensembl
Innerchr9:107917721..107920618hg38UCSC Ensembl
Outerchr9:107917658..107920681hg38UCSC Ensembl
chr9:110679970..110682930hg19UCSC Ensembl
Innerchr9:110680002..110682899hg19UCSC Ensembl
Outerchr9:110679939..110682962hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382961
hg192961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621412
Supporting Variants
SamplesHG03784
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13594645
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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