A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283436



Internal ID20492654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73563828..73563828hg38UCSC Ensembl
chr6:74273551..74273551hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283436
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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