A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621957



Internal ID7008823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134245815..134270075hg38UCSC Ensembl
chr9:137137661..137161921hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3824261
hg1924261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13641434
SamplesHG01061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621957
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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