A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6236819



Internal ID9295124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133495690..133496082hg38UCSC Ensembl
chr9:136360812..136361204hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656592
Supporting Variants
SamplesNA12842
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6236819
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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