A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13594573



Internal ID2300016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107895787..107900577hg38UCSC Ensembl
chr9:110658068..110662858hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg384791
hg194791
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621409
Supporting Variants
SamplesHG02052
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13594573
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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