A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621697



Internal ID7008564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123686587..123690198hg38UCSC Ensembl
Innerchr9:123686587..123690198hg38UCSC Ensembl
Outerchr9:123686482..123690332hg38UCSC Ensembl
chr9:126448866..126452477hg19UCSC Ensembl
Innerchr9:126448866..126452477hg19UCSC Ensembl
Outerchr9:126448761..126452611hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383612
hg193612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618482
SamplesHG01936
Known GenesDENND1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621697
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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