A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102262



Internal ID22011498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40629784..40629784hg38UCSC Ensembl
chr19:41135689..41135689hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632428
Samples
Known GenesLTBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102262
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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