A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656816



Internal ID9922921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121583094..121589404hg38UCSC Ensembl
chr9:124345373..124351683hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg386311
hg196311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6069780
SamplesNA19463
Known GenesDAB2IP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656816
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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