A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620983



Internal ID6661164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87690200..87691658hg38UCSC Ensembl
Innerchr9:87690204..87691655hg38UCSC Ensembl
Outerchr9:87690197..87691662hg38UCSC Ensembl
chr9:90305115..90306573hg19UCSC Ensembl
Innerchr9:90305119..90306570hg19UCSC Ensembl
Outerchr9:90305112..90306577hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13548022, essv13548021
SamplesHG03028, HG02628
Known GenesDAPK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620983
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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