A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677308



Internal ID9596727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74531842..74532474hg38UCSC Ensembl
Outerchr9:74531805..74532524hg38UCSC Ensembl
Innerchr9:77146758..77147390hg19UCSC Ensembl
Outerchr9:77146721..77147440hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5907396
SamplesNA18977
Known GenesMIR6130, RORB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677308
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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