A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6284522



Internal ID8954444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8600791..8602478hg38UCSC Ensembl
Outerchr19:8600634..8602631hg38UCSC Ensembl
Innerchr19:8665675..8667362hg19UCSC Ensembl
Outerchr19:8665518..8667515hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381998
hg191998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667281
Supporting Variants
SamplesHG00513
Known GenesADAMTS10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6284522
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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