A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051224



Internal ID21960457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43935881..43935881hg38UCSC Ensembl
chr2:44163020..44163020hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522612
Samples
Known GenesLRPPRC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051224
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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