A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075632



Internal ID21481410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64171757..64171981hg38UCSC Ensembl
chr11:63939229..63939453hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587055
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075632
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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