A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672805



Internal ID9592224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3835764..3836569hg38UCSC Ensembl
chr9:3835764..3836569hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6590573
SamplesNA19676
Known GenesGLIS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672805
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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