A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043750



Internal ID21953044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116271415..116271415hg38UCSC Ensembl
chr1:116814037..116814037hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043750
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer