A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075431



Internal ID21503577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66166427..66171858hg38UCSC Ensembl
chr11:65933898..65939329hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385432
hg195432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592011
Supporting Variants
SamplesNA19239
Known GenesPACS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075431
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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