A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958274



Internal ID22733348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70845656..70845656hg38UCSC Ensembl
chr10:72605413..72605413hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358369
Samples
Known GenesSGPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958274
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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