A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657658



Internal ID9577077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19110536..19140638hg38UCSC Ensembl
Outerchr9:19110499..19140688hg38UCSC Ensembl
Innerchr9:19110534..19140636hg19UCSC Ensembl
Outerchr9:19110497..19140686hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3830190
hg1930190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5434719
SamplesHG00737
Known GenesPLIN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657658
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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