A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032465



Internal ID89336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14695465..14695465hg38UCSC Ensembl
chr10:14737464..14737464hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551164
Supporting Variants
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032465
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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