A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969816



Internal ID22744751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119135791..119135791hg38UCSC Ensembl
chr10:120895303..120895303hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366435
Samples
Known GenesFAM45A, FAM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969816
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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