A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620816



Internal ID7007686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78879922..79031998hg38UCSC Ensembl
chr9:81494838..81646914hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38152077
hg19152077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13533531
SamplesHG00478
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620816
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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