A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451197



Internal ID22509069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9361035..9363769hg38UCSC Ensembl
chr11:9382582..9385316hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382735
hg192735
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451197
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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