A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072193



Internal ID21465545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118518941..118519002hg38UCSC Ensembl
chr11:118389656..118389717hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589062
Supporting Variants
SamplesHG03065
Known GenesKMT2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072193
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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