A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621635



Internal ID7008503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119491637..119507634hg38UCSC Ensembl
Innerchr9:119492137..119507134hg38UCSC Ensembl
Outerchr9:119490637..119508634hg38UCSC Ensembl
chr9:122253915..122269912hg19UCSC Ensembl
Innerchr9:122254415..122269412hg19UCSC Ensembl
Outerchr9:122252915..122270912hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3815998
hg1915998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13613193
SamplesHG03945
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621635
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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