A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621349



Internal ID7008218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104975220..104992894hg38UCSC Ensembl
chr9:107737501..107755175hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3817675
hg1917675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1499e214
Supporting Variantsessv13592543
SamplesHG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621349
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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