A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619961



Internal ID6660146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21284070..21306754hg38UCSC Ensembl
Innerchr9:21284070..21306754hg38UCSC Ensembl
Outerchr9:21283570..21307254hg38UCSC Ensembl
chr9:21284069..21306753hg19UCSC Ensembl
Innerchr9:21284069..21306753hg19UCSC Ensembl
Outerchr9:21283569..21307253hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3822685
hg1922685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13419709
SamplesNA18912
Known GenesIFNA5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619961
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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