A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953603



Internal ID22728882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155753313..155753313hg38UCSC Ensembl
chr5:155132873..155132873hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953603
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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