A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461776



Internal ID22519661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17348609..17355758hg38UCSC Ensembl
chr11:17370156..17377305hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387150
hg197150
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859269
Supporting Variants
Samples
Known GenesNCR3LG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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