A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665611



Internal ID9931716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128429546..128434056hg38UCSC Ensembl
Outerchr9:128429509..128434106hg38UCSC Ensembl
Innerchr9:131191825..131196335hg19UCSC Ensembl
Outerchr9:131191788..131196385hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384598
hg194598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1378e199
Supporting Variantsessv6591172
SamplesNA19472
Known GenesCERCAM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665611
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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