A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076164



Internal ID21477933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76567796..76567868hg38UCSC Ensembl
chr11:76278840..76278912hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599977
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076164
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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