A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055738



Internal ID104990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8656638..8656648hg38UCSC Ensembl
chr12:8809234..8809244hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546700
Supporting Variants
Samples
Known GenesMFAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055738
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.029459


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