A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13420786



Internal ID5314245
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619969
Supporting Variants
SamplesNA18864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13420786
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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