A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13428628



Internal ID6261733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23290061..23299939hg38UCSC Ensembl
Innerchr9:23290061..23299939hg38UCSC Ensembl
Outerchr9:23289738..23300188hg38UCSC Ensembl
chr9:23290059..23299937hg19UCSC Ensembl
Innerchr9:23290059..23299937hg19UCSC Ensembl
Outerchr9:23289736..23300186hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389879
hg199879
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620011
Supporting Variants
SamplesNA19782
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13428628
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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