A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045192



Internal ID21954462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121824839..121824839hg38UCSC Ensembl
chr1:121360399..121360399hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045192
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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