A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050950



Internal ID21960184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15834242..15834242hg38UCSC Ensembl
chr1:16160737..16160737hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530856
Samples
Known GenesFLJ37453
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050950
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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