A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621218



Internal ID7008087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99019438..99022092hg38UCSC Ensembl
Innerchr9:99019452..99022078hg38UCSC Ensembl
Outerchr9:99019424..99022106hg38UCSC Ensembl
chr9:101781720..101784374hg19UCSC Ensembl
Innerchr9:101781734..101784360hg19UCSC Ensembl
Outerchr9:101781706..101784388hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382655
hg192655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13579214, essv13579213
SamplesHG00306, NA19113
Known GenesCOL15A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621218
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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