A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955895



Internal ID22731091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43564427..43564427hg38UCSC Ensembl
chr5:43564529..43564529hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955895
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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