A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621809



Internal ID7008675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128447993..128454564hg38UCSC Ensembl
Innerchr9:128447993..128454564hg38UCSC Ensembl
Outerchr9:128447711..128454966hg38UCSC Ensembl
chr9:131210272..131216843hg19UCSC Ensembl
Innerchr9:131210272..131216843hg19UCSC Ensembl
Outerchr9:131209990..131217245hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386572
hg196572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13622828, essv13622829
SamplesHG03907, HG00595
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621809
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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