A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619966



Internal ID7006839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21650013..21655792hg38UCSC Ensembl
Innerchr9:21650013..21655792hg38UCSC Ensembl
Outerchr9:21649788..21655997hg38UCSC Ensembl
chr9:21650012..21655791hg19UCSC Ensembl
Innerchr9:21650012..21655791hg19UCSC Ensembl
Outerchr9:21649787..21655996hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385780
hg195780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13419720
SamplesHG01354
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619966
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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