A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459671



Internal ID22517557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78524970..78582415hg38UCSC Ensembl
chr11:78236016..78293460hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3857446
hg1957445
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866852
Supporting Variants
Samples
Known GenesNARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459671
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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