A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351953



Internal ID22577622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57304632..57304827hg38UCSC Ensembl
chr11:57072106..57072301hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912951
Supporting Variants
Samples
Known GenesTNKS1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351953
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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