A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071961



Internal ID21981194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149130881..149130881hg38UCSC Ensembl
chr3:148848668..148848668hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543938
Samples
Known GenesHPS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071961
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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