A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621956



Internal ID7008822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134245815..134270075hg38UCSC Ensembl
chr9:137137661..137161921hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3824261
hg1924261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13641433
SamplesNA19449
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621956
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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