A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045625



Internal ID21954889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9535568..9535568hg38UCSC Ensembl
chr3:9577252..9577252hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528522
Samples
Known GenesLHFPL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045625
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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