A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621642



Internal ID7008510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120074302..120124727hg38UCSC Ensembl
Innerchr9:120074329..120124701hg38UCSC Ensembl
Outerchr9:120074276..120124754hg38UCSC Ensembl
chr9:122836580..122887005hg19UCSC Ensembl
Innerchr9:122836607..122886979hg19UCSC Ensembl
Outerchr9:122836554..122887032hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3850426
hg1950426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1508e214
Supporting Variantsessv13613205, essv13613206
SamplesHG00881, HG00851
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621642
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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