A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13593255



Internal ID5027821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105610038..105611160hg38UCSC Ensembl
Innerchr9:105610038..105611160hg38UCSC Ensembl
Outerchr9:105609759..105611322hg38UCSC Ensembl
chr9:108372319..108373441hg19UCSC Ensembl
Innerchr9:108372319..108373441hg19UCSC Ensembl
Outerchr9:108372040..108373603hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621359
Supporting Variants
SamplesNA18519
Known GenesFKTN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13593255
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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