A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950955



Internal ID22726344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32543791..32543791hg38UCSC Ensembl
chr5:32543897..32543897hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950955
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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