A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621202



Internal ID6661381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98071613..98109713hg38UCSC Ensembl
Innerchr9:98072113..98109213hg38UCSC Ensembl
Outerchr9:98070613..98110713hg38UCSC Ensembl
chr9:100833895..100871995hg19UCSC Ensembl
Innerchr9:100834395..100871495hg19UCSC Ensembl
Outerchr9:100832895..100872995hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3838101
hg1938101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1495e214
Supporting Variantsessv13574313
SamplesHG01767
Known GenesNANS, TRIM14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621202
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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