A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667995



Internal ID9587414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84704339..84706593hg38UCSC Ensembl
Outerchr9:84704302..84706643hg38UCSC Ensembl
Innerchr9:87319254..87321508hg19UCSC Ensembl
Outerchr9:87319217..87321558hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382342
hg192342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6532925
SamplesHG00656
Known GenesNTRK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667995
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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