A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043930



Internal ID21953221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9940742..9940742hg38UCSC Ensembl
chr3:9982426..9982426hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524746
Samples
Known GenesCRELD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043930
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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