A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043982



Internal ID21953273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155792239..155792239hg38UCSC Ensembl
chr1:155762030..155762030hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529419
Samples
Known GenesGON4L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043982
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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