A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13508897



Internal ID4429024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69264300..69271959hg38UCSC Ensembl
chr9:71879216..71886875hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg387660
hg197660
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620555
Supporting Variants
SamplesHG03943
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13508897
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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