A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5808000



Internal ID9174894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137440164..137442220hg38UCSC Ensembl
Outerchr9:137439793..137442640hg38UCSC Ensembl
Innerchr9:140334616..140336672hg19UCSC Ensembl
Outerchr9:140334245..140337092hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657589
Supporting Variants
SamplesHG01383
Known GenesENTPD8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5808000
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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