A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961601



Internal ID22736548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72555274..72555274hg38UCSC Ensembl
chr3:72604425..72604425hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961601
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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