A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075414



Internal ID21413800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65842768..65843040hg38UCSC Ensembl
chr11:65610239..65610511hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601565
Supporting Variants
SamplesHG00513
Known GenesSNX32
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075414
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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