A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363127



Internal ID22588796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14184298..14184298hg38UCSC Ensembl
chr10:14226297..14226297hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962493
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363127
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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