A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073292



Internal ID21982525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41049358..41049358hg38UCSC Ensembl
chr4:41051375..41051375hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537790
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073292
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