A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658382



Internal ID9577801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92580171..92582720hg38UCSC Ensembl
Outerchr9:92580134..92582770hg38UCSC Ensembl
Innerchr9:95342453..95345002hg19UCSC Ensembl
Outerchr9:95342416..95345052hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382637
hg192637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6390408
SamplesNA19900
Known GenesCENPP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658382
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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