A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620981



Internal ID6661162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87519496..87522470hg38UCSC Ensembl
Innerchr9:87519537..87522429hg38UCSC Ensembl
Outerchr9:87519455..87522511hg38UCSC Ensembl
chr9:90134411..90137385hg19UCSC Ensembl
Innerchr9:90134452..90137344hg19UCSC Ensembl
Outerchr9:90134370..90137426hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382975
hg192975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13548019
SamplesHG02798
Known GenesDAPK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620981
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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