A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619969



Internal ID7006842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21758253..21769773hg38UCSC Ensembl
Innerchr9:21758314..21769713hg38UCSC Ensembl
Outerchr9:21758193..21769834hg38UCSC Ensembl
chr9:21758252..21769772hg19UCSC Ensembl
Innerchr9:21758313..21769712hg19UCSC Ensembl
Outerchr9:21758192..21769833hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3811521
hg1911521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13420786
SamplesNA18864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619969
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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