A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6122490



Internal ID9892210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2141541..2142631hg38UCSC Ensembl
chr9:2141541..2142631hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676342
Supporting Variants
SamplesNA20772
Known GenesSMARCA2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6122490
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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