A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656914



Internal ID9576333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76298124..76300082hg38UCSC Ensembl
chr17:74294205..74296163hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381959
hg191959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6449919
SamplesNA11893
Known GenesQRICH2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656914
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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