A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103324



Internal ID22012558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47761340..47761340hg38UCSC Ensembl
chr19:48264597..48264597hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103324
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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