A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966941



Internal ID22741876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151534970..151534970hg38UCSC Ensembl
chr5:150914531..150914531hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415451
Samples
Known GenesFAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966941
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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