A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350466



Internal ID22576135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73203051..73203989hg38UCSC Ensembl
chr11:72914096..72915034hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350466
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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