A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13591673



Internal ID2682549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104442351..104460718hg38UCSC Ensembl
chr9:107204632..107222999hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3818368
hg1918368
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621330
Supporting Variants
SamplesHG02375
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13591673
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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