A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621920



Internal ID6662096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132716365..132845220hg38UCSC Ensembl
chr9:135591752..135720607hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38128856
hg19128856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1513e214
Supporting Variantsessv13635935
SamplesHG00131
Known GenesAK8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621920
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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