A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13432348



Internal ID6752067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25056942..25125390hg38UCSC Ensembl
Innerchr9:25056942..25125390hg38UCSC Ensembl
Outerchr9:25056442..25125890hg38UCSC Ensembl
chr9:25056940..25125388hg19UCSC Ensembl
Innerchr9:25056940..25125388hg19UCSC Ensembl
Outerchr9:25056440..25125888hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3868449
hg1968449
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620062
Supporting Variants
SamplesNA20866
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13432348
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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