A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621710



Internal ID7008577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124104999..124110776hg38UCSC Ensembl
Innerchr9:124105016..124110759hg38UCSC Ensembl
Outerchr9:124104982..124110793hg38UCSC Ensembl
chr9:126867278..126873055hg19UCSC Ensembl
Innerchr9:126867295..126873038hg19UCSC Ensembl
Outerchr9:126867261..126873072hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385778
hg195778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618643
SamplesNA19740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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