A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621772



Internal ID7008638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126798961..126804500hg38UCSC Ensembl
Innerchr9:126798997..126804464hg38UCSC Ensembl
Outerchr9:126798925..126804536hg38UCSC Ensembl
chr9:129561240..129566779hg19UCSC Ensembl
Innerchr9:129561276..129566743hg19UCSC Ensembl
Outerchr9:129561204..129566815hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385540
hg195540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13621604
SamplesNA19456
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621772
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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