A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5726508



Internal ID8703911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137634225..137729111hg38UCSC Ensembl
Outerchr9:137634188..137729161hg38UCSC Ensembl
Innerchr9:140528677..140623563hg19UCSC Ensembl
Outerchr9:140528640..140623613hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3894974
hg1994974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675080
Supporting Variants
SamplesHG01342
Known GenesEHMT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5726508
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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