A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966429



Internal ID22741364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71065399..71065399hg38UCSC Ensembl
chr4:71931116..71931116hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966429
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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