A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13526645



Internal ID4853613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75201604..75358572hg38UCSC Ensembl
chr9:77816520..77973488hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38156969
hg19156969
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620717
Supporting Variants
SamplesNA12273
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13526645
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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