A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13482487



Internal ID6405749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42730139..42763058hg38UCSC Ensembl
chr9:44208061..44240980hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3832920
hg1932920
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620486
Supporting Variants
SamplesNA20355
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13482487
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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